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nsv471625

  • Variant Calls:25
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:159,114

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 1640 SVs from 105 studies. See in: genome view    
Remapped(Score: Perfect):69,250,956-69,410,069Question Mark
Overlapping variant regions from other studies: 1640 SVs from 105 studies. See in: genome view    
Remapped(Score: Perfect):70,116,674-70,275,787Question Mark
Overlapping variant regions from other studies: 7 SVs from 4 studies. See in: genome view    
Submitted genomic70,432,219-70,591,332Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nsv471625RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000004.12Chr469,250,95669,410,069
nsv471625RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr470,116,67470,275,787
nsv471625Submitted genomicNCBI34 (hg16)Primary AssemblyNC_000004.8Chr470,432,21970,591,332

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv549285copy number lossGM10469ABAC aCGHProbe signal intensity56
nssv549286copy number lossGM10470ABAC aCGHProbe signal intensity49
nssv549287copy number lossGM10492ABAC aCGHProbe signal intensity47
nssv549288copy number lossGM10493BAC aCGHProbe signal intensity65
nssv549289copy number lossGM10494ABAC aCGHProbe signal intensity55
nssv549290copy number lossGM10495BBAC aCGHProbe signal intensity45
nssv549291copy number lossGM10496ABAC aCGHProbe signal intensity59
nssv549292copy number lossGM10967BAC aCGHProbe signal intensity58
nssv549293copy number lossGM10970BAC aCGHProbe signal intensity55
nssv549294copy number lossGM10971BAC aCGHProbe signal intensity56
nssv549295copy number lossGM10976BAC aCGHProbe signal intensity56
nssv549296copy number lossGM10979BAC aCGHProbe signal intensity65
nssv549297copy number lossGM11323BAC aCGHProbe signal intensity53
nssv549298copy number lossGM11521BAC aCGHProbe signal intensity49
nssv549299copy number lossGM11523BAC aCGHProbe signal intensity54
nssv549300copy number lossGM16689BAC aCGHProbe signal intensity42
nssv549301copy number lossGM17015BAC aCGHProbe signal intensity60
nssv549302copy number lossGM17051BAC aCGHProbe signal intensity54
nssv549303copy number lossGM17052BAC aCGHProbe signal intensity50
nssv549304copy number lossGM17058BAC aCGHProbe signal intensity54
nssv549305copy number lossJK1058BBAC aCGHProbe signal intensity61
nssv549306copy number lossJK1061BAC aCGHProbe signal intensity51
nssv549307copy number lossJK1688BBAC aCGHProbe signal intensity53
nssv549308copy number lossJK776BAC aCGHProbe signal intensity50
nssv549309copy number lossP86GABAC aCGHProbe signal intensity50

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
nssv549285RemappedPerfectNC_000004.12:g.(?_
69250956)_(6941006
9_?)del
GRCh38.p12First PassNC_000004.12Chr469,250,95669,410,069
nssv549286RemappedPerfectNC_000004.12:g.(?_
69250956)_(6941006
9_?)del
GRCh38.p12First PassNC_000004.12Chr469,250,95669,410,069
nssv549287RemappedPerfectNC_000004.12:g.(?_
69250956)_(6941006
9_?)del
GRCh38.p12First PassNC_000004.12Chr469,250,95669,410,069
nssv549288RemappedPerfectNC_000004.12:g.(?_
69250956)_(6941006
9_?)del
GRCh38.p12First PassNC_000004.12Chr469,250,95669,410,069
nssv549289RemappedPerfectNC_000004.12:g.(?_
69250956)_(6941006
9_?)del
GRCh38.p12First PassNC_000004.12Chr469,250,95669,410,069
nssv549290RemappedPerfectNC_000004.12:g.(?_
69250956)_(6941006
9_?)del
GRCh38.p12First PassNC_000004.12Chr469,250,95669,410,069
nssv549291RemappedPerfectNC_000004.12:g.(?_
69250956)_(6941006
9_?)del
GRCh38.p12First PassNC_000004.12Chr469,250,95669,410,069
nssv549292RemappedPerfectNC_000004.12:g.(?_
69250956)_(6941006
9_?)del
GRCh38.p12First PassNC_000004.12Chr469,250,95669,410,069
nssv549293RemappedPerfectNC_000004.12:g.(?_
69250956)_(6941006
9_?)del
GRCh38.p12First PassNC_000004.12Chr469,250,95669,410,069
nssv549294RemappedPerfectNC_000004.12:g.(?_
69250956)_(6941006
9_?)del
GRCh38.p12First PassNC_000004.12Chr469,250,95669,410,069
nssv549295RemappedPerfectNC_000004.12:g.(?_
69250956)_(6941006
9_?)del
GRCh38.p12First PassNC_000004.12Chr469,250,95669,410,069
nssv549296RemappedPerfectNC_000004.12:g.(?_
69250956)_(6941006
9_?)del
GRCh38.p12First PassNC_000004.12Chr469,250,95669,410,069
nssv549297RemappedPerfectNC_000004.12:g.(?_
69250956)_(6941006
9_?)del
GRCh38.p12First PassNC_000004.12Chr469,250,95669,410,069
nssv549298RemappedPerfectNC_000004.12:g.(?_
69250956)_(6941006
9_?)del
GRCh38.p12First PassNC_000004.12Chr469,250,95669,410,069
nssv549299RemappedPerfectNC_000004.12:g.(?_
69250956)_(6941006
9_?)del
GRCh38.p12First PassNC_000004.12Chr469,250,95669,410,069
nssv549300RemappedPerfectNC_000004.12:g.(?_
69250956)_(6941006
9_?)del
GRCh38.p12First PassNC_000004.12Chr469,250,95669,410,069
nssv549301RemappedPerfectNC_000004.12:g.(?_
69250956)_(6941006
9_?)del
GRCh38.p12First PassNC_000004.12Chr469,250,95669,410,069
nssv549302RemappedPerfectNC_000004.12:g.(?_
69250956)_(6941006
9_?)del
GRCh38.p12First PassNC_000004.12Chr469,250,95669,410,069
nssv549303RemappedPerfectNC_000004.12:g.(?_
69250956)_(6941006
9_?)del
GRCh38.p12First PassNC_000004.12Chr469,250,95669,410,069
nssv549304RemappedPerfectNC_000004.12:g.(?_
69250956)_(6941006
9_?)del
GRCh38.p12First PassNC_000004.12Chr469,250,95669,410,069
nssv549305RemappedPerfectNC_000004.12:g.(?_
69250956)_(6941006
9_?)del
GRCh38.p12First PassNC_000004.12Chr469,250,95669,410,069
nssv549306RemappedPerfectNC_000004.12:g.(?_
69250956)_(6941006
9_?)del
GRCh38.p12First PassNC_000004.12Chr469,250,95669,410,069
nssv549307RemappedPerfectNC_000004.12:g.(?_
69250956)_(6941006
9_?)del
GRCh38.p12First PassNC_000004.12Chr469,250,95669,410,069
nssv549308RemappedPerfectNC_000004.12:g.(?_
69250956)_(6941006
9_?)del
GRCh38.p12First PassNC_000004.12Chr469,250,95669,410,069
nssv549309RemappedPerfectNC_000004.12:g.(?_
69250956)_(6941006
9_?)del
GRCh38.p12First PassNC_000004.12Chr469,250,95669,410,069
nssv549285RemappedPerfectNC_000004.11:g.(?_
70116674)_(7027578
7_?)del
GRCh37.p13First PassNC_000004.11Chr470,116,67470,275,787
nssv549286RemappedPerfectNC_000004.11:g.(?_
70116674)_(7027578
7_?)del
GRCh37.p13First PassNC_000004.11Chr470,116,67470,275,787
nssv549287RemappedPerfectNC_000004.11:g.(?_
70116674)_(7027578
7_?)del
GRCh37.p13First PassNC_000004.11Chr470,116,67470,275,787
nssv549288RemappedPerfectNC_000004.11:g.(?_
70116674)_(7027578
7_?)del
GRCh37.p13First PassNC_000004.11Chr470,116,67470,275,787
nssv549289RemappedPerfectNC_000004.11:g.(?_
70116674)_(7027578
7_?)del
GRCh37.p13First PassNC_000004.11Chr470,116,67470,275,787
nssv549290RemappedPerfectNC_000004.11:g.(?_
70116674)_(7027578
7_?)del
GRCh37.p13First PassNC_000004.11Chr470,116,67470,275,787
nssv549291RemappedPerfectNC_000004.11:g.(?_
70116674)_(7027578
7_?)del
GRCh37.p13First PassNC_000004.11Chr470,116,67470,275,787
nssv549292RemappedPerfectNC_000004.11:g.(?_
70116674)_(7027578
7_?)del
GRCh37.p13First PassNC_000004.11Chr470,116,67470,275,787
nssv549293RemappedPerfectNC_000004.11:g.(?_
70116674)_(7027578
7_?)del
GRCh37.p13First PassNC_000004.11Chr470,116,67470,275,787
nssv549294RemappedPerfectNC_000004.11:g.(?_
70116674)_(7027578
7_?)del
GRCh37.p13First PassNC_000004.11Chr470,116,67470,275,787
nssv549295RemappedPerfectNC_000004.11:g.(?_
70116674)_(7027578
7_?)del
GRCh37.p13First PassNC_000004.11Chr470,116,67470,275,787
nssv549296RemappedPerfectNC_000004.11:g.(?_
70116674)_(7027578
7_?)del
GRCh37.p13First PassNC_000004.11Chr470,116,67470,275,787
nssv549297RemappedPerfectNC_000004.11:g.(?_
70116674)_(7027578
7_?)del
GRCh37.p13First PassNC_000004.11Chr470,116,67470,275,787
nssv549298RemappedPerfectNC_000004.11:g.(?_
70116674)_(7027578
7_?)del
GRCh37.p13First PassNC_000004.11Chr470,116,67470,275,787
nssv549299RemappedPerfectNC_000004.11:g.(?_
70116674)_(7027578
7_?)del
GRCh37.p13First PassNC_000004.11Chr470,116,67470,275,787
nssv549300RemappedPerfectNC_000004.11:g.(?_
70116674)_(7027578
7_?)del
GRCh37.p13First PassNC_000004.11Chr470,116,67470,275,787
nssv549301RemappedPerfectNC_000004.11:g.(?_
70116674)_(7027578
7_?)del
GRCh37.p13First PassNC_000004.11Chr470,116,67470,275,787
nssv549302RemappedPerfectNC_000004.11:g.(?_
70116674)_(7027578
7_?)del
GRCh37.p13First PassNC_000004.11Chr470,116,67470,275,787
nssv549303RemappedPerfectNC_000004.11:g.(?_
70116674)_(7027578
7_?)del
GRCh37.p13First PassNC_000004.11Chr470,116,67470,275,787
nssv549304RemappedPerfectNC_000004.11:g.(?_
70116674)_(7027578
7_?)del
GRCh37.p13First PassNC_000004.11Chr470,116,67470,275,787
nssv549305RemappedPerfectNC_000004.11:g.(?_
70116674)_(7027578
7_?)del
GRCh37.p13First PassNC_000004.11Chr470,116,67470,275,787
nssv549306RemappedPerfectNC_000004.11:g.(?_
70116674)_(7027578
7_?)del
GRCh37.p13First PassNC_000004.11Chr470,116,67470,275,787
nssv549307RemappedPerfectNC_000004.11:g.(?_
70116674)_(7027578
7_?)del
GRCh37.p13First PassNC_000004.11Chr470,116,67470,275,787
nssv549308RemappedPerfectNC_000004.11:g.(?_
70116674)_(7027578
7_?)del
GRCh37.p13First PassNC_000004.11Chr470,116,67470,275,787
nssv549309RemappedPerfectNC_000004.11:g.(?_
70116674)_(7027578
7_?)del
GRCh37.p13First PassNC_000004.11Chr470,116,67470,275,787
nssv549285Submitted genomicNC_000004.8:g.(?_7
0432219)_(70591332
_?)del
NCBI34 (hg16)NC_000004.8Chr470,432,21970,591,332
nssv549286Submitted genomicNC_000004.8:g.(?_7
0432219)_(70591332
_?)del
NCBI34 (hg16)NC_000004.8Chr470,432,21970,591,332
nssv549287Submitted genomicNC_000004.8:g.(?_7
0432219)_(70591332
_?)del
NCBI34 (hg16)NC_000004.8Chr470,432,21970,591,332
nssv549288Submitted genomicNC_000004.8:g.(?_7
0432219)_(70591332
_?)del
NCBI34 (hg16)NC_000004.8Chr470,432,21970,591,332
nssv549289Submitted genomicNC_000004.8:g.(?_7
0432219)_(70591332
_?)del
NCBI34 (hg16)NC_000004.8Chr470,432,21970,591,332
nssv549290Submitted genomicNC_000004.8:g.(?_7
0432219)_(70591332
_?)del
NCBI34 (hg16)NC_000004.8Chr470,432,21970,591,332
nssv549291Submitted genomicNC_000004.8:g.(?_7
0432219)_(70591332
_?)del
NCBI34 (hg16)NC_000004.8Chr470,432,21970,591,332
nssv549292Submitted genomicNC_000004.8:g.(?_7
0432219)_(70591332
_?)del
NCBI34 (hg16)NC_000004.8Chr470,432,21970,591,332
nssv549293Submitted genomicNC_000004.8:g.(?_7
0432219)_(70591332
_?)del
NCBI34 (hg16)NC_000004.8Chr470,432,21970,591,332
nssv549294Submitted genomicNC_000004.8:g.(?_7
0432219)_(70591332
_?)del
NCBI34 (hg16)NC_000004.8Chr470,432,21970,591,332
nssv549295Submitted genomicNC_000004.8:g.(?_7
0432219)_(70591332
_?)del
NCBI34 (hg16)NC_000004.8Chr470,432,21970,591,332
nssv549296Submitted genomicNC_000004.8:g.(?_7
0432219)_(70591332
_?)del
NCBI34 (hg16)NC_000004.8Chr470,432,21970,591,332
nssv549297Submitted genomicNC_000004.8:g.(?_7
0432219)_(70591332
_?)del
NCBI34 (hg16)NC_000004.8Chr470,432,21970,591,332
nssv549298Submitted genomicNC_000004.8:g.(?_7
0432219)_(70591332
_?)del
NCBI34 (hg16)NC_000004.8Chr470,432,21970,591,332
nssv549299Submitted genomicNC_000004.8:g.(?_7
0432219)_(70591332
_?)del
NCBI34 (hg16)NC_000004.8Chr470,432,21970,591,332
nssv549300Submitted genomicNC_000004.8:g.(?_7
0432219)_(70591332
_?)del
NCBI34 (hg16)NC_000004.8Chr470,432,21970,591,332
nssv549301Submitted genomicNC_000004.8:g.(?_7
0432219)_(70591332
_?)del
NCBI34 (hg16)NC_000004.8Chr470,432,21970,591,332
nssv549302Submitted genomicNC_000004.8:g.(?_7
0432219)_(70591332
_?)del
NCBI34 (hg16)NC_000004.8Chr470,432,21970,591,332
nssv549303Submitted genomicNC_000004.8:g.(?_7
0432219)_(70591332
_?)del
NCBI34 (hg16)NC_000004.8Chr470,432,21970,591,332
nssv549304Submitted genomicNC_000004.8:g.(?_7
0432219)_(70591332
_?)del
NCBI34 (hg16)NC_000004.8Chr470,432,21970,591,332
nssv549305Submitted genomicNC_000004.8:g.(?_7
0432219)_(70591332
_?)del
NCBI34 (hg16)NC_000004.8Chr470,432,21970,591,332
nssv549306Submitted genomicNC_000004.8:g.(?_7
0432219)_(70591332
_?)del
NCBI34 (hg16)NC_000004.8Chr470,432,21970,591,332
nssv549307Submitted genomicNC_000004.8:g.(?_7
0432219)_(70591332
_?)del
NCBI34 (hg16)NC_000004.8Chr470,432,21970,591,332
nssv549308Submitted genomicNC_000004.8:g.(?_7
0432219)_(70591332
_?)del
NCBI34 (hg16)NC_000004.8Chr470,432,21970,591,332
nssv549309Submitted genomicNC_000004.8:g.(?_7
0432219)_(70591332
_?)del
NCBI34 (hg16)NC_000004.8Chr470,432,21970,591,332

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

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