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nsv1046695

  • Variant Calls:19
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:251,227

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 934 SVs from 92 studies. See in: genome view    
Remapped(Score: Perfect):67,730,549-67,981,775Question Mark
Overlapping variant regions from other studies: 930 SVs from 92 studies. See in: genome view    
Remapped(Score: Perfect):67,498,020-67,749,246Question Mark
Overlapping variant regions from other studies: 271 SVs from 25 studies. See in: genome view    
Submitted genomic67,254,596-67,505,822Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nsv1046695RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000011.10Chr1167,730,54967,981,775
nsv1046695RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1167,498,02067,749,246
nsv1046695Submitted genomicNCBI36 (hg18)Primary AssemblyNC_000011.8Chr1167,254,59667,505,822

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv3507512copy number gainSNP arrayProbe signal intensity
nssv3509098copy number gainSNP arrayProbe signal intensity
nssv3509890copy number gainSNP arrayProbe signal intensity
nssv3510794copy number gainSNP arrayProbe signal intensity
nssv3512607copy number gainSNP arrayProbe signal intensity
nssv3515113copy number gainSNP arrayProbe signal intensity
nssv3516014copy number gainSNP arrayProbe signal intensity
nssv3516887copy number gainSNP arrayProbe signal intensity
nssv3518879copy number gainSNP arrayProbe signal intensity
nssv3518896copy number lossSNP arrayProbe signal intensity
nssv3519774copy number gainSNP arrayProbe signal intensity
nssv3521397copy number gainSNP arrayProbe signal intensity
nssv3521720copy number gainSNP arrayProbe signal intensity
nssv3710627copy number gainSNP arrayProbe signal intensity
nssv3710628copy number gainSNP arrayProbe signal intensity
nssv3710629copy number gainSNP arrayProbe signal intensity
nssv3710630copy number gainSNP arrayProbe signal intensity
nssv3710631copy number gainSNP arrayProbe signal intensity
nssv3710632copy number gainSNP arrayProbe signal intensity

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
nssv3507512RemappedPerfectNC_000011.10:g.(?_
67730549)_(6798177
5_?)dup
GRCh38.p12First PassNC_000011.10Chr1167,730,54967,981,775
nssv3509098RemappedPerfectNC_000011.10:g.(?_
67730549)_(6798177
5_?)dup
GRCh38.p12First PassNC_000011.10Chr1167,730,54967,981,775
nssv3509890RemappedPerfectNC_000011.10:g.(?_
67730549)_(6798177
5_?)dup
GRCh38.p12First PassNC_000011.10Chr1167,730,54967,981,775
nssv3510794RemappedPerfectNC_000011.10:g.(?_
67730549)_(6798177
5_?)dup
GRCh38.p12First PassNC_000011.10Chr1167,730,54967,981,775
nssv3512607RemappedPerfectNC_000011.10:g.(?_
67730549)_(6798177
5_?)dup
GRCh38.p12First PassNC_000011.10Chr1167,730,54967,981,775
nssv3515113RemappedPerfectNC_000011.10:g.(?_
67730549)_(6798177
5_?)dup
GRCh38.p12First PassNC_000011.10Chr1167,730,54967,981,775
nssv3516014RemappedPerfectNC_000011.10:g.(?_
67730549)_(6798177
5_?)dup
GRCh38.p12First PassNC_000011.10Chr1167,730,54967,981,775
nssv3516887RemappedPerfectNC_000011.10:g.(?_
67730549)_(6798177
5_?)dup
GRCh38.p12First PassNC_000011.10Chr1167,730,54967,981,775
nssv3518879RemappedPerfectNC_000011.10:g.(?_
67730549)_(6798177
5_?)dup
GRCh38.p12First PassNC_000011.10Chr1167,730,54967,981,775
nssv3518896RemappedPerfectNC_000011.10:g.(?_
67730549)_(6798177
5_?)del
GRCh38.p12First PassNC_000011.10Chr1167,730,54967,981,775
nssv3519774RemappedPerfectNC_000011.10:g.(?_
67730549)_(6798177
5_?)dup
GRCh38.p12First PassNC_000011.10Chr1167,730,54967,981,775
nssv3521397RemappedPerfectNC_000011.10:g.(?_
67730549)_(6798177
5_?)dup
GRCh38.p12First PassNC_000011.10Chr1167,730,54967,981,775
nssv3521720RemappedPerfectNC_000011.10:g.(?_
67730549)_(6798177
5_?)dup
GRCh38.p12First PassNC_000011.10Chr1167,730,54967,981,775
nssv3710627RemappedPerfectNC_000011.10:g.(?_
67730549)_(6798177
5_?)dup
GRCh38.p12First PassNC_000011.10Chr1167,730,54967,981,775
nssv3710628RemappedPerfectNC_000011.10:g.(?_
67730549)_(6798177
5_?)dup
GRCh38.p12First PassNC_000011.10Chr1167,730,54967,981,775
nssv3710629RemappedPerfectNC_000011.10:g.(?_
67730549)_(6798177
5_?)dup
GRCh38.p12First PassNC_000011.10Chr1167,730,54967,981,775
nssv3710630RemappedPerfectNC_000011.10:g.(?_
67730549)_(6798177
5_?)dup
GRCh38.p12First PassNC_000011.10Chr1167,730,54967,981,775
nssv3710631RemappedPerfectNC_000011.10:g.(?_
67730549)_(6798177
5_?)dup
GRCh38.p12First PassNC_000011.10Chr1167,730,54967,981,775
nssv3710632RemappedPerfectNC_000011.10:g.(?_
67730549)_(6798177
5_?)dup
GRCh38.p12First PassNC_000011.10Chr1167,730,54967,981,775
nssv3507512RemappedPerfectNC_000011.9:g.(?_6
7498020)_(67749246
_?)dup
GRCh37.p13First PassNC_000011.9Chr1167,498,02067,749,246
nssv3509098RemappedPerfectNC_000011.9:g.(?_6
7498020)_(67749246
_?)dup
GRCh37.p13First PassNC_000011.9Chr1167,498,02067,749,246
nssv3509890RemappedPerfectNC_000011.9:g.(?_6
7498020)_(67749246
_?)dup
GRCh37.p13First PassNC_000011.9Chr1167,498,02067,749,246
nssv3510794RemappedPerfectNC_000011.9:g.(?_6
7498020)_(67749246
_?)dup
GRCh37.p13First PassNC_000011.9Chr1167,498,02067,749,246
nssv3512607RemappedPerfectNC_000011.9:g.(?_6
7498020)_(67749246
_?)dup
GRCh37.p13First PassNC_000011.9Chr1167,498,02067,749,246
nssv3515113RemappedPerfectNC_000011.9:g.(?_6
7498020)_(67749246
_?)dup
GRCh37.p13First PassNC_000011.9Chr1167,498,02067,749,246
nssv3516014RemappedPerfectNC_000011.9:g.(?_6
7498020)_(67749246
_?)dup
GRCh37.p13First PassNC_000011.9Chr1167,498,02067,749,246
nssv3516887RemappedPerfectNC_000011.9:g.(?_6
7498020)_(67749246
_?)dup
GRCh37.p13First PassNC_000011.9Chr1167,498,02067,749,246
nssv3518879RemappedPerfectNC_000011.9:g.(?_6
7498020)_(67749246
_?)dup
GRCh37.p13First PassNC_000011.9Chr1167,498,02067,749,246
nssv3518896RemappedPerfectNC_000011.9:g.(?_6
7498020)_(67749246
_?)del
GRCh37.p13First PassNC_000011.9Chr1167,498,02067,749,246
nssv3519774RemappedPerfectNC_000011.9:g.(?_6
7498020)_(67749246
_?)dup
GRCh37.p13First PassNC_000011.9Chr1167,498,02067,749,246
nssv3521397RemappedPerfectNC_000011.9:g.(?_6
7498020)_(67749246
_?)dup
GRCh37.p13First PassNC_000011.9Chr1167,498,02067,749,246
nssv3521720RemappedPerfectNC_000011.9:g.(?_6
7498020)_(67749246
_?)dup
GRCh37.p13First PassNC_000011.9Chr1167,498,02067,749,246
nssv3710627RemappedPerfectNC_000011.9:g.(?_6
7498020)_(67749246
_?)dup
GRCh37.p13First PassNC_000011.9Chr1167,498,02067,749,246
nssv3710628RemappedPerfectNC_000011.9:g.(?_6
7498020)_(67749246
_?)dup
GRCh37.p13First PassNC_000011.9Chr1167,498,02067,749,246
nssv3710629RemappedPerfectNC_000011.9:g.(?_6
7498020)_(67749246
_?)dup
GRCh37.p13First PassNC_000011.9Chr1167,498,02067,749,246
nssv3710630RemappedPerfectNC_000011.9:g.(?_6
7498020)_(67749246
_?)dup
GRCh37.p13First PassNC_000011.9Chr1167,498,02067,749,246
nssv3710631RemappedPerfectNC_000011.9:g.(?_6
7498020)_(67749246
_?)dup
GRCh37.p13First PassNC_000011.9Chr1167,498,02067,749,246
nssv3710632RemappedPerfectNC_000011.9:g.(?_6
7498020)_(67749246
_?)dup
GRCh37.p13First PassNC_000011.9Chr1167,498,02067,749,246
nssv3507512Submitted genomicNC_000011.8:g.(?_6
7254596)_(67505822
_?)dup
NCBI36 (hg18)NC_000011.8Chr1167,254,59667,505,822
nssv3509098Submitted genomicNC_000011.8:g.(?_6
7254596)_(67505822
_?)dup
NCBI36 (hg18)NC_000011.8Chr1167,254,59667,505,822
nssv3509890Submitted genomicNC_000011.8:g.(?_6
7254596)_(67505822
_?)dup
NCBI36 (hg18)NC_000011.8Chr1167,254,59667,505,822
nssv3510794Submitted genomicNC_000011.8:g.(?_6
7254596)_(67505822
_?)dup
NCBI36 (hg18)NC_000011.8Chr1167,254,59667,505,822
nssv3512607Submitted genomicNC_000011.8:g.(?_6
7254596)_(67505822
_?)dup
NCBI36 (hg18)NC_000011.8Chr1167,254,59667,505,822
nssv3515113Submitted genomicNC_000011.8:g.(?_6
7254596)_(67505822
_?)dup
NCBI36 (hg18)NC_000011.8Chr1167,254,59667,505,822
nssv3516014Submitted genomicNC_000011.8:g.(?_6
7254596)_(67505822
_?)dup
NCBI36 (hg18)NC_000011.8Chr1167,254,59667,505,822
nssv3516887Submitted genomicNC_000011.8:g.(?_6
7254596)_(67505822
_?)dup
NCBI36 (hg18)NC_000011.8Chr1167,254,59667,505,822
nssv3518879Submitted genomicNC_000011.8:g.(?_6
7254596)_(67505822
_?)dup
NCBI36 (hg18)NC_000011.8Chr1167,254,59667,505,822
nssv3518896Submitted genomicNC_000011.8:g.(?_6
7254596)_(67505822
_?)del
NCBI36 (hg18)NC_000011.8Chr1167,254,59667,505,822
nssv3519774Submitted genomicNC_000011.8:g.(?_6
7254596)_(67505822
_?)dup
NCBI36 (hg18)NC_000011.8Chr1167,254,59667,505,822
nssv3521397Submitted genomicNC_000011.8:g.(?_6
7254596)_(67505822
_?)dup
NCBI36 (hg18)NC_000011.8Chr1167,254,59667,505,822
nssv3521720Submitted genomicNC_000011.8:g.(?_6
7254596)_(67505822
_?)dup
NCBI36 (hg18)NC_000011.8Chr1167,254,59667,505,822
nssv3710627Submitted genomicNC_000011.8:g.(?_6
7254596)_(67505822
_?)dup
NCBI36 (hg18)NC_000011.8Chr1167,254,59667,505,822
nssv3710628Submitted genomicNC_000011.8:g.(?_6
7254596)_(67505822
_?)dup
NCBI36 (hg18)NC_000011.8Chr1167,254,59667,505,822
nssv3710629Submitted genomicNC_000011.8:g.(?_6
7254596)_(67505822
_?)dup
NCBI36 (hg18)NC_000011.8Chr1167,254,59667,505,822
nssv3710630Submitted genomicNC_000011.8:g.(?_6
7254596)_(67505822
_?)dup
NCBI36 (hg18)NC_000011.8Chr1167,254,59667,505,822
nssv3710631Submitted genomicNC_000011.8:g.(?_6
7254596)_(67505822
_?)dup
NCBI36 (hg18)NC_000011.8Chr1167,254,59667,505,822
nssv3710632Submitted genomicNC_000011.8:g.(?_6
7254596)_(67505822
_?)dup
NCBI36 (hg18)NC_000011.8Chr1167,254,59667,505,822

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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