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nsv833775

  • Variant Calls:16
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:176,314

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 793 SVs from 72 studies. See in: genome view    
Remapped(Score: Perfect):18,102,951-18,279,264Question Mark
Overlapping variant regions from other studies: 793 SVs from 72 studies. See in: genome view    
Remapped(Score: Perfect):18,213,761-18,390,074Question Mark
Overlapping variant regions from other studies: 27 SVs from 3 studies. See in: genome view    
Submitted genomic18,074,761-18,251,074Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartOuter Stop
nsv833775RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000019.10Chr1918,102,95118,279,264
nsv833775RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1918,213,76118,390,074
nsv833775Submitted genomicNCBI35 (hg17)Primary AssemblyNC_000019.8Chr1918,074,76118,251,074

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv1454594copy number lossBAC aCGHProbe signal intensity
nssv1454595copy number lossBAC aCGHProbe signal intensity
nssv1454596copy number lossBAC aCGHProbe signal intensity
nssv1454597copy number lossBAC aCGHProbe signal intensity
nssv1454598copy number lossBAC aCGHProbe signal intensity
nssv1454599copy number lossBAC aCGHProbe signal intensity
nssv1454600copy number lossBAC aCGHProbe signal intensity
nssv1454601copy number lossBAC aCGHProbe signal intensity
nssv1454602copy number lossBAC aCGHProbe signal intensity
nssv1454603copy number lossBAC aCGHProbe signal intensity
nssv1454604copy number lossBAC aCGHProbe signal intensity
nssv1454605copy number lossBAC aCGHProbe signal intensity
nssv1454606copy number lossBAC aCGHProbe signal intensity
nssv1454607copy number lossBAC aCGHProbe signal intensity
nssv1454608copy number lossBAC aCGHProbe signal intensity
nssv1454609copy number lossBAC aCGHProbe signal intensity

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartOuter Stop
nssv1454594RemappedPerfectNC_000019.10:g.(18
102951_?)_(?_18279
264)del
GRCh38.p12First PassNC_000019.10Chr1918,102,95118,279,264
nssv1454595RemappedPerfectNC_000019.10:g.(18
102951_?)_(?_18279
264)del
GRCh38.p12First PassNC_000019.10Chr1918,102,95118,279,264
nssv1454596RemappedPerfectNC_000019.10:g.(18
102951_?)_(?_18279
264)del
GRCh38.p12First PassNC_000019.10Chr1918,102,95118,279,264
nssv1454597RemappedPerfectNC_000019.10:g.(18
102951_?)_(?_18279
264)del
GRCh38.p12First PassNC_000019.10Chr1918,102,95118,279,264
nssv1454598RemappedPerfectNC_000019.10:g.(18
102951_?)_(?_18279
264)del
GRCh38.p12First PassNC_000019.10Chr1918,102,95118,279,264
nssv1454599RemappedPerfectNC_000019.10:g.(18
102951_?)_(?_18279
264)del
GRCh38.p12First PassNC_000019.10Chr1918,102,95118,279,264
nssv1454600RemappedPerfectNC_000019.10:g.(18
102951_?)_(?_18279
264)del
GRCh38.p12First PassNC_000019.10Chr1918,102,95118,279,264
nssv1454601RemappedPerfectNC_000019.10:g.(18
102951_?)_(?_18279
264)del
GRCh38.p12First PassNC_000019.10Chr1918,102,95118,279,264
nssv1454602RemappedPerfectNC_000019.10:g.(18
102951_?)_(?_18279
264)del
GRCh38.p12First PassNC_000019.10Chr1918,102,95118,279,264
nssv1454603RemappedPerfectNC_000019.10:g.(18
102951_?)_(?_18279
264)del
GRCh38.p12First PassNC_000019.10Chr1918,102,95118,279,264
nssv1454604RemappedPerfectNC_000019.10:g.(18
102951_?)_(?_18279
264)del
GRCh38.p12First PassNC_000019.10Chr1918,102,95118,279,264
nssv1454605RemappedPerfectNC_000019.10:g.(18
102951_?)_(?_18279
264)del
GRCh38.p12First PassNC_000019.10Chr1918,102,95118,279,264
nssv1454606RemappedPerfectNC_000019.10:g.(18
102951_?)_(?_18279
264)del
GRCh38.p12First PassNC_000019.10Chr1918,102,95118,279,264
nssv1454607RemappedPerfectNC_000019.10:g.(18
102951_?)_(?_18279
264)del
GRCh38.p12First PassNC_000019.10Chr1918,102,95118,279,264
nssv1454608RemappedPerfectNC_000019.10:g.(18
102951_?)_(?_18279
264)del
GRCh38.p12First PassNC_000019.10Chr1918,102,95118,279,264
nssv1454609RemappedPerfectNC_000019.10:g.(18
102951_?)_(?_18279
264)del
GRCh38.p12First PassNC_000019.10Chr1918,102,95118,279,264
nssv1454594RemappedPerfectNC_000019.9:g.(182
13761_?)_(?_183900
74)del
GRCh37.p13First PassNC_000019.9Chr1918,213,76118,390,074
nssv1454595RemappedPerfectNC_000019.9:g.(182
13761_?)_(?_183900
74)del
GRCh37.p13First PassNC_000019.9Chr1918,213,76118,390,074
nssv1454596RemappedPerfectNC_000019.9:g.(182
13761_?)_(?_183900
74)del
GRCh37.p13First PassNC_000019.9Chr1918,213,76118,390,074
nssv1454597RemappedPerfectNC_000019.9:g.(182
13761_?)_(?_183900
74)del
GRCh37.p13First PassNC_000019.9Chr1918,213,76118,390,074
nssv1454598RemappedPerfectNC_000019.9:g.(182
13761_?)_(?_183900
74)del
GRCh37.p13First PassNC_000019.9Chr1918,213,76118,390,074
nssv1454599RemappedPerfectNC_000019.9:g.(182
13761_?)_(?_183900
74)del
GRCh37.p13First PassNC_000019.9Chr1918,213,76118,390,074
nssv1454600RemappedPerfectNC_000019.9:g.(182
13761_?)_(?_183900
74)del
GRCh37.p13First PassNC_000019.9Chr1918,213,76118,390,074
nssv1454601RemappedPerfectNC_000019.9:g.(182
13761_?)_(?_183900
74)del
GRCh37.p13First PassNC_000019.9Chr1918,213,76118,390,074
nssv1454602RemappedPerfectNC_000019.9:g.(182
13761_?)_(?_183900
74)del
GRCh37.p13First PassNC_000019.9Chr1918,213,76118,390,074
nssv1454603RemappedPerfectNC_000019.9:g.(182
13761_?)_(?_183900
74)del
GRCh37.p13First PassNC_000019.9Chr1918,213,76118,390,074
nssv1454604RemappedPerfectNC_000019.9:g.(182
13761_?)_(?_183900
74)del
GRCh37.p13First PassNC_000019.9Chr1918,213,76118,390,074
nssv1454605RemappedPerfectNC_000019.9:g.(182
13761_?)_(?_183900
74)del
GRCh37.p13First PassNC_000019.9Chr1918,213,76118,390,074
nssv1454606RemappedPerfectNC_000019.9:g.(182
13761_?)_(?_183900
74)del
GRCh37.p13First PassNC_000019.9Chr1918,213,76118,390,074
nssv1454607RemappedPerfectNC_000019.9:g.(182
13761_?)_(?_183900
74)del
GRCh37.p13First PassNC_000019.9Chr1918,213,76118,390,074
nssv1454608RemappedPerfectNC_000019.9:g.(182
13761_?)_(?_183900
74)del
GRCh37.p13First PassNC_000019.9Chr1918,213,76118,390,074
nssv1454609RemappedPerfectNC_000019.9:g.(182
13761_?)_(?_183900
74)del
GRCh37.p13First PassNC_000019.9Chr1918,213,76118,390,074
nssv1454594Submitted genomicNC_000019.8:g.(180
74761_?)_(?_182510
74)del
NCBI35 (hg17)NC_000019.8Chr1918,074,76118,251,074
nssv1454595Submitted genomicNC_000019.8:g.(180
74761_?)_(?_182510
74)del
NCBI35 (hg17)NC_000019.8Chr1918,074,76118,251,074
nssv1454596Submitted genomicNC_000019.8:g.(180
74761_?)_(?_182510
74)del
NCBI35 (hg17)NC_000019.8Chr1918,074,76118,251,074
nssv1454597Submitted genomicNC_000019.8:g.(180
74761_?)_(?_182510
74)del
NCBI35 (hg17)NC_000019.8Chr1918,074,76118,251,074
nssv1454598Submitted genomicNC_000019.8:g.(180
74761_?)_(?_182510
74)del
NCBI35 (hg17)NC_000019.8Chr1918,074,76118,251,074
nssv1454599Submitted genomicNC_000019.8:g.(180
74761_?)_(?_182510
74)del
NCBI35 (hg17)NC_000019.8Chr1918,074,76118,251,074
nssv1454600Submitted genomicNC_000019.8:g.(180
74761_?)_(?_182510
74)del
NCBI35 (hg17)NC_000019.8Chr1918,074,76118,251,074
nssv1454601Submitted genomicNC_000019.8:g.(180
74761_?)_(?_182510
74)del
NCBI35 (hg17)NC_000019.8Chr1918,074,76118,251,074
nssv1454602Submitted genomicNC_000019.8:g.(180
74761_?)_(?_182510
74)del
NCBI35 (hg17)NC_000019.8Chr1918,074,76118,251,074
nssv1454603Submitted genomicNC_000019.8:g.(180
74761_?)_(?_182510
74)del
NCBI35 (hg17)NC_000019.8Chr1918,074,76118,251,074
nssv1454604Submitted genomicNC_000019.8:g.(180
74761_?)_(?_182510
74)del
NCBI35 (hg17)NC_000019.8Chr1918,074,76118,251,074
nssv1454605Submitted genomicNC_000019.8:g.(180
74761_?)_(?_182510
74)del
NCBI35 (hg17)NC_000019.8Chr1918,074,76118,251,074
nssv1454606Submitted genomicNC_000019.8:g.(180
74761_?)_(?_182510
74)del
NCBI35 (hg17)NC_000019.8Chr1918,074,76118,251,074
nssv1454607Submitted genomicNC_000019.8:g.(180
74761_?)_(?_182510
74)del
NCBI35 (hg17)NC_000019.8Chr1918,074,76118,251,074
nssv1454608Submitted genomicNC_000019.8:g.(180
74761_?)_(?_182510
74)del
NCBI35 (hg17)NC_000019.8Chr1918,074,76118,251,074
nssv1454609Submitted genomicNC_000019.8:g.(180
74761_?)_(?_182510
74)del
NCBI35 (hg17)NC_000019.8Chr1918,074,76118,251,074

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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