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nsv428386

  • Variant Calls:23
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:266,880

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 1166 SVs from 87 studies. See in: genome view    
Remapped(Score: Perfect):21,328,921-21,595,800Question Mark
Overlapping variant regions from other studies: 1166 SVs from 87 studies. See in: genome view    
Remapped(Score: Perfect):21,683,210-21,950,089Question Mark
Overlapping variant regions from other studies: 512 SVs from 26 studies. See in: genome view    
Submitted genomic20,013,210-20,280,089Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nsv428386RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000022.11Chr2221,328,92121,595,800
nsv428386RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000022.10Chr2221,683,21021,950,089
nsv428386Submitted genomicNCBI36 (hg18)Primary AssemblyNC_000022.9Chr2220,013,21020,280,089

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv453965copy number lossHGDP00450BAC aCGHProbe signal intensity88
nssv453966copy number lossHGDP00460BAC aCGHProbe signal intensity67
nssv453967copy number lossHGDP00471BAC aCGHProbe signal intensity73
nssv453968copy number lossHGDP00473BAC aCGHProbe signal intensity64
nssv453969copy number lossNA19189BAC aCGHProbe signal intensity94
nssv453970copy number lossNA19225BAC aCGHProbe signal intensity71
nssv453971copy number lossHGDP00449BAC aCGHProbe signal intensity126
nssv453972copy number lossHGDP00462BAC aCGHProbe signal intensity83
nssv453973copy number lossHGDP00463BAC aCGHProbe signal intensity90
nssv453974copy number lossHGDP00472BAC aCGHProbe signal intensity65
nssv453976copy number lossHGDP00984BAC aCGHProbe signal intensity75
nssv453977copy number lossHGDP00986BAC aCGHProbe signal intensity82
nssv453978copy number lossHGDP01087BAC aCGHProbe signal intensity75
nssv453979copy number lossHGDP01088BAC aCGHProbe signal intensity78
nssv453980copy number lossHGDP01089BAC aCGHProbe signal intensity65
nssv453981copy number lossHGDP01093BAC aCGHProbe signal intensity95
nssv453982copy number lossHGDP01094BAC aCGHProbe signal intensity92
nssv453983copy number lossNA18498BAC aCGHProbe signal intensity97
nssv453984copy number lossNA18916BAC aCGHProbe signal intensity90
nssv453985copy number lossNA19096BAC aCGHProbe signal intensity100
nssv453987copy number lossNA19113BAC aCGHProbe signal intensity122
nssv453988copy number lossNA19181BAC aCGHProbe signal intensity87
nssv453989copy number lossNA19257BAC aCGHProbe signal intensity86

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
nssv453965RemappedPerfectNC_000022.11:g.(?_
21328921)_(2145144
9_?)del
GRCh38.p12First PassNC_000022.11Chr2221,328,92121,451,449
nssv453966RemappedPerfectNC_000022.11:g.(?_
21328921)_(2145144
9_?)del
GRCh38.p12First PassNC_000022.11Chr2221,328,92121,451,449
nssv453967RemappedPerfectNC_000022.11:g.(?_
21328921)_(2145144
9_?)del
GRCh38.p12First PassNC_000022.11Chr2221,328,92121,451,449
nssv453968RemappedPerfectNC_000022.11:g.(?_
21328921)_(2145144
9_?)del
GRCh38.p12First PassNC_000022.11Chr2221,328,92121,451,449
nssv453969RemappedPerfectNC_000022.11:g.(?_
21328921)_(2145144
9_?)del
GRCh38.p12First PassNC_000022.11Chr2221,328,92121,451,449
nssv453970RemappedPerfectNC_000022.11:g.(?_
21328921)_(2145144
9_?)del
GRCh38.p12First PassNC_000022.11Chr2221,328,92121,451,449
nssv453971RemappedPerfectNC_000022.11:g.(?_
21328921)_(2159580
0_?)del
GRCh38.p12First PassNC_000022.11Chr2221,328,92121,595,800
nssv453972RemappedPerfectNC_000022.11:g.(?_
21328921)_(2159580
0_?)del
GRCh38.p12First PassNC_000022.11Chr2221,328,92121,595,800
nssv453973RemappedPerfectNC_000022.11:g.(?_
21328921)_(2159580
0_?)del
GRCh38.p12First PassNC_000022.11Chr2221,328,92121,595,800
nssv453974RemappedPerfectNC_000022.11:g.(?_
21328921)_(2159580
0_?)del
GRCh38.p12First PassNC_000022.11Chr2221,328,92121,595,800
nssv453976RemappedPerfectNC_000022.11:g.(?_
21328921)_(2159580
0_?)del
GRCh38.p12First PassNC_000022.11Chr2221,328,92121,595,800
nssv453977RemappedPerfectNC_000022.11:g.(?_
21328921)_(2159580
0_?)del
GRCh38.p12First PassNC_000022.11Chr2221,328,92121,595,800
nssv453978RemappedPerfectNC_000022.11:g.(?_
21328921)_(2159580
0_?)del
GRCh38.p12First PassNC_000022.11Chr2221,328,92121,595,800
nssv453979RemappedPerfectNC_000022.11:g.(?_
21328921)_(2159580
0_?)del
GRCh38.p12First PassNC_000022.11Chr2221,328,92121,595,800
nssv453980RemappedPerfectNC_000022.11:g.(?_
21328921)_(2159580
0_?)del
GRCh38.p12First PassNC_000022.11Chr2221,328,92121,595,800
nssv453981RemappedPerfectNC_000022.11:g.(?_
21328921)_(2159580
0_?)del
GRCh38.p12First PassNC_000022.11Chr2221,328,92121,595,800
nssv453982RemappedPerfectNC_000022.11:g.(?_
21328921)_(2159580
0_?)del
GRCh38.p12First PassNC_000022.11Chr2221,328,92121,595,800
nssv453983RemappedPerfectNC_000022.11:g.(?_
21328921)_(2159580
0_?)del
GRCh38.p12First PassNC_000022.11Chr2221,328,92121,595,800
nssv453984RemappedPerfectNC_000022.11:g.(?_
21328921)_(2159580
0_?)del
GRCh38.p12First PassNC_000022.11Chr2221,328,92121,595,800
nssv453985RemappedPerfectNC_000022.11:g.(?_
21328921)_(2159580
0_?)del
GRCh38.p12First PassNC_000022.11Chr2221,328,92121,595,800
nssv453987RemappedPerfectNC_000022.11:g.(?_
21328921)_(2159580
0_?)del
GRCh38.p12First PassNC_000022.11Chr2221,328,92121,595,800
nssv453988RemappedPerfectNC_000022.11:g.(?_
21328921)_(2159580
0_?)del
GRCh38.p12First PassNC_000022.11Chr2221,328,92121,595,800
nssv453989RemappedPerfectNC_000022.11:g.(?_
21328921)_(2159580
0_?)del
GRCh38.p12First PassNC_000022.11Chr2221,328,92121,595,800
nssv453965RemappedPerfectNC_000022.10:g.(?_
21683210)_(2180573
8_?)del
GRCh37.p13First PassNC_000022.10Chr2221,683,21021,805,738
nssv453966RemappedPerfectNC_000022.10:g.(?_
21683210)_(2180573
8_?)del
GRCh37.p13First PassNC_000022.10Chr2221,683,21021,805,738
nssv453967RemappedPerfectNC_000022.10:g.(?_
21683210)_(2180573
8_?)del
GRCh37.p13First PassNC_000022.10Chr2221,683,21021,805,738
nssv453968RemappedPerfectNC_000022.10:g.(?_
21683210)_(2180573
8_?)del
GRCh37.p13First PassNC_000022.10Chr2221,683,21021,805,738
nssv453969RemappedPerfectNC_000022.10:g.(?_
21683210)_(2180573
8_?)del
GRCh37.p13First PassNC_000022.10Chr2221,683,21021,805,738
nssv453970RemappedPerfectNC_000022.10:g.(?_
21683210)_(2180573
8_?)del
GRCh37.p13First PassNC_000022.10Chr2221,683,21021,805,738
nssv453971RemappedPerfectNC_000022.10:g.(?_
21683210)_(2195008
9_?)del
GRCh37.p13First PassNC_000022.10Chr2221,683,21021,950,089
nssv453972RemappedPerfectNC_000022.10:g.(?_
21683210)_(2195008
9_?)del
GRCh37.p13First PassNC_000022.10Chr2221,683,21021,950,089
nssv453973RemappedPerfectNC_000022.10:g.(?_
21683210)_(2195008
9_?)del
GRCh37.p13First PassNC_000022.10Chr2221,683,21021,950,089
nssv453974RemappedPerfectNC_000022.10:g.(?_
21683210)_(2195008
9_?)del
GRCh37.p13First PassNC_000022.10Chr2221,683,21021,950,089
nssv453976RemappedPerfectNC_000022.10:g.(?_
21683210)_(2195008
9_?)del
GRCh37.p13First PassNC_000022.10Chr2221,683,21021,950,089
nssv453977RemappedPerfectNC_000022.10:g.(?_
21683210)_(2195008
9_?)del
GRCh37.p13First PassNC_000022.10Chr2221,683,21021,950,089
nssv453978RemappedPerfectNC_000022.10:g.(?_
21683210)_(2195008
9_?)del
GRCh37.p13First PassNC_000022.10Chr2221,683,21021,950,089
nssv453979RemappedPerfectNC_000022.10:g.(?_
21683210)_(2195008
9_?)del
GRCh37.p13First PassNC_000022.10Chr2221,683,21021,950,089
nssv453980RemappedPerfectNC_000022.10:g.(?_
21683210)_(2195008
9_?)del
GRCh37.p13First PassNC_000022.10Chr2221,683,21021,950,089
nssv453981RemappedPerfectNC_000022.10:g.(?_
21683210)_(2195008
9_?)del
GRCh37.p13First PassNC_000022.10Chr2221,683,21021,950,089
nssv453982RemappedPerfectNC_000022.10:g.(?_
21683210)_(2195008
9_?)del
GRCh37.p13First PassNC_000022.10Chr2221,683,21021,950,089
nssv453983RemappedPerfectNC_000022.10:g.(?_
21683210)_(2195008
9_?)del
GRCh37.p13First PassNC_000022.10Chr2221,683,21021,950,089
nssv453984RemappedPerfectNC_000022.10:g.(?_
21683210)_(2195008
9_?)del
GRCh37.p13First PassNC_000022.10Chr2221,683,21021,950,089
nssv453985RemappedPerfectNC_000022.10:g.(?_
21683210)_(2195008
9_?)del
GRCh37.p13First PassNC_000022.10Chr2221,683,21021,950,089
nssv453987RemappedPerfectNC_000022.10:g.(?_
21683210)_(2195008
9_?)del
GRCh37.p13First PassNC_000022.10Chr2221,683,21021,950,089
nssv453988RemappedPerfectNC_000022.10:g.(?_
21683210)_(2195008
9_?)del
GRCh37.p13First PassNC_000022.10Chr2221,683,21021,950,089
nssv453989RemappedPerfectNC_000022.10:g.(?_
21683210)_(2195008
9_?)del
GRCh37.p13First PassNC_000022.10Chr2221,683,21021,950,089
nssv453965Submitted genomicNC_000022.9:g.(?_2
0013210)_(20135738
_?)del
NCBI36 (hg18)NC_000022.9Chr2220,013,21020,135,738
nssv453966Submitted genomicNC_000022.9:g.(?_2
0013210)_(20135738
_?)del
NCBI36 (hg18)NC_000022.9Chr2220,013,21020,135,738
nssv453967Submitted genomicNC_000022.9:g.(?_2
0013210)_(20135738
_?)del
NCBI36 (hg18)NC_000022.9Chr2220,013,21020,135,738
nssv453968Submitted genomicNC_000022.9:g.(?_2
0013210)_(20135738
_?)del
NCBI36 (hg18)NC_000022.9Chr2220,013,21020,135,738
nssv453969Submitted genomicNC_000022.9:g.(?_2
0013210)_(20135738
_?)del
NCBI36 (hg18)NC_000022.9Chr2220,013,21020,135,738
nssv453970Submitted genomicNC_000022.9:g.(?_2
0013210)_(20135738
_?)del
NCBI36 (hg18)NC_000022.9Chr2220,013,21020,135,738
nssv453971Submitted genomicNC_000022.9:g.(?_2
0013210)_(20280089
_?)del
NCBI36 (hg18)NC_000022.9Chr2220,013,21020,280,089
nssv453972Submitted genomicNC_000022.9:g.(?_2
0013210)_(20280089
_?)del
NCBI36 (hg18)NC_000022.9Chr2220,013,21020,280,089
nssv453973Submitted genomicNC_000022.9:g.(?_2
0013210)_(20280089
_?)del
NCBI36 (hg18)NC_000022.9Chr2220,013,21020,280,089
nssv453974Submitted genomicNC_000022.9:g.(?_2
0013210)_(20280089
_?)del
NCBI36 (hg18)NC_000022.9Chr2220,013,21020,280,089
nssv453976Submitted genomicNC_000022.9:g.(?_2
0013210)_(20280089
_?)del
NCBI36 (hg18)NC_000022.9Chr2220,013,21020,280,089
nssv453977Submitted genomicNC_000022.9:g.(?_2
0013210)_(20280089
_?)del
NCBI36 (hg18)NC_000022.9Chr2220,013,21020,280,089
nssv453978Submitted genomicNC_000022.9:g.(?_2
0013210)_(20280089
_?)del
NCBI36 (hg18)NC_000022.9Chr2220,013,21020,280,089
nssv453979Submitted genomicNC_000022.9:g.(?_2
0013210)_(20280089
_?)del
NCBI36 (hg18)NC_000022.9Chr2220,013,21020,280,089
nssv453980Submitted genomicNC_000022.9:g.(?_2
0013210)_(20280089
_?)del
NCBI36 (hg18)NC_000022.9Chr2220,013,21020,280,089
nssv453981Submitted genomicNC_000022.9:g.(?_2
0013210)_(20280089
_?)del
NCBI36 (hg18)NC_000022.9Chr2220,013,21020,280,089
nssv453982Submitted genomicNC_000022.9:g.(?_2
0013210)_(20280089
_?)del
NCBI36 (hg18)NC_000022.9Chr2220,013,21020,280,089
nssv453983Submitted genomicNC_000022.9:g.(?_2
0013210)_(20280089
_?)del
NCBI36 (hg18)NC_000022.9Chr2220,013,21020,280,089
nssv453984Submitted genomicNC_000022.9:g.(?_2
0013210)_(20280089
_?)del
NCBI36 (hg18)NC_000022.9Chr2220,013,21020,280,089
nssv453985Submitted genomicNC_000022.9:g.(?_2
0013210)_(20280089
_?)del
NCBI36 (hg18)NC_000022.9Chr2220,013,21020,280,089
nssv453987Submitted genomicNC_000022.9:g.(?_2
0013210)_(20280089
_?)del
NCBI36 (hg18)NC_000022.9Chr2220,013,21020,280,089
nssv453988Submitted genomicNC_000022.9:g.(?_2
0013210)_(20280089
_?)del
NCBI36 (hg18)NC_000022.9Chr2220,013,21020,280,089
nssv453989Submitted genomicNC_000022.9:g.(?_2
0013210)_(20280089
_?)del
NCBI36 (hg18)NC_000022.9Chr2220,013,21020,280,089

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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