U.S. flag

An official website of the United States government

nsv897250

  • Variant Calls:18
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:91,079

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 499 SVs from 69 studies. See in: genome view    
Remapped(Score: Perfect):38,227,656-38,318,734Question Mark
Overlapping variant regions from other studies: 499 SVs from 69 studies. See in: genome view    
Remapped(Score: Perfect):38,249,206-38,340,284Question Mark
Overlapping variant regions from other studies: 191 SVs from 26 studies. See in: genome view    
Submitted genomic38,205,782-38,296,860Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
nsv897250RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000011.10Chr1138,227,65638,230,63538,304,83338,318,734
nsv897250RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1138,249,20638,252,18538,326,38338,340,284
nsv897250Submitted genomicNCBI36 (hg18)Primary AssemblyNC_000011.8Chr1138,205,78238,208,76138,282,95938,296,860

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv1532048copy number lossMS10699SNP arraySNP genotyping analysis39
nssv1532157copy number lossMS10727SNP arraySNP genotyping analysis29
nssv1532680copy number lossMS10802SNP arraySNP genotyping analysis73
nssv1535583copy number lossMS12266SNP arraySNP genotyping analysis58
nssv1551347copy number lossMS18847SNP arraySNP genotyping analysis113
nssv1552859copy number lossMS19634SNP arraySNP genotyping analysis77
nssv1554634copy number lossMS20872SNP arraySNP genotyping analysis79
nssv1556349copy number lossMS21928SNP arraySNP genotyping analysis9
nssv1556630copy number lossMS22104SNP arraySNP genotyping analysis139
nssv1558996copy number lossMS23670SNP arraySNP genotyping analysis55
nssv1563971copy number gainIS30139SNP arraySNP genotyping analysis7
nssv1570135copy number lossIS31812SNP arraySNP genotyping analysis21
nssv1577773copy number gainIS34555SNP arraySNP genotyping analysis23
nssv1581850copy number lossIS35742SNP arraySNP genotyping analysis62
nssv1583065copy number lossIS36244SNP arraySNP genotyping analysis54
nssv1588661copy number lossIS38231SNP arraySNP genotyping analysis19
nssv1594894copy number gainIS40057SNP arraySNP genotyping analysis8
nssv1597676copy number lossIS41224SNP arraySNP genotyping analysis51

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
nssv1532048RemappedPerfectNC_000011.10:g.(38
227656_38230635)_(
38304833_38318734)
del
GRCh38.p12First PassNC_000011.10Chr1138,227,65638,230,63538,304,83338,318,734
nssv1532157RemappedPerfectNC_000011.10:g.(38
227656_38230635)_(
38304833_38318734)
del
GRCh38.p12First PassNC_000011.10Chr1138,227,65638,230,63538,304,83338,318,734
nssv1532680RemappedPerfectNC_000011.10:g.(38
227656_38230635)_(
38304833_38318734)
del
GRCh38.p12First PassNC_000011.10Chr1138,227,65638,230,63538,304,83338,318,734
nssv1535583RemappedPerfectNC_000011.10:g.(38
227656_38230635)_(
38304833_38318734)
del
GRCh38.p12First PassNC_000011.10Chr1138,227,65638,230,63538,304,83338,318,734
nssv1551347RemappedPerfectNC_000011.10:g.(38
227656_38230635)_(
38304833_38318734)
del
GRCh38.p12First PassNC_000011.10Chr1138,227,65638,230,63538,304,83338,318,734
nssv1552859RemappedPerfectNC_000011.10:g.(38
227656_38230635)_(
38304833_38318734)
del
GRCh38.p12First PassNC_000011.10Chr1138,227,65638,230,63538,304,83338,318,734
nssv1554634RemappedPerfectNC_000011.10:g.(38
227656_38230635)_(
38304833_38318734)
del
GRCh38.p12First PassNC_000011.10Chr1138,227,65638,230,63538,304,83338,318,734
nssv1556349RemappedPerfectNC_000011.10:g.(38
227656_38230635)_(
38304833_38318734)
del
GRCh38.p12First PassNC_000011.10Chr1138,227,65638,230,63538,304,83338,318,734
nssv1556630RemappedPerfectNC_000011.10:g.(38
227656_38230635)_(
38304833_38318734)
del
GRCh38.p12First PassNC_000011.10Chr1138,227,65638,230,63538,304,83338,318,734
nssv1558996RemappedPerfectNC_000011.10:g.(38
227656_38230635)_(
38304833_38318734)
del
GRCh38.p12First PassNC_000011.10Chr1138,227,65638,230,63538,304,83338,318,734
nssv1563971RemappedPerfectNC_000011.10:g.(38
227656_38230635)_(
38304833_38318734)
dup
GRCh38.p12First PassNC_000011.10Chr1138,227,65638,230,63538,304,83338,318,734
nssv1570135RemappedPerfectNC_000011.10:g.(38
227656_38230635)_(
38304833_38318734)
del
GRCh38.p12First PassNC_000011.10Chr1138,227,65638,230,63538,304,83338,318,734
nssv1577773RemappedPerfectNC_000011.10:g.(38
227656_38230635)_(
38304833_38318734)
dup
GRCh38.p12First PassNC_000011.10Chr1138,227,65638,230,63538,304,83338,318,734
nssv1581850RemappedPerfectNC_000011.10:g.(38
227656_38230635)_(
38304833_38318734)
del
GRCh38.p12First PassNC_000011.10Chr1138,227,65638,230,63538,304,83338,318,734
nssv1583065RemappedPerfectNC_000011.10:g.(38
227656_38230635)_(
38304833_38318734)
del
GRCh38.p12First PassNC_000011.10Chr1138,227,65638,230,63538,304,83338,318,734
nssv1588661RemappedPerfectNC_000011.10:g.(38
227656_38230635)_(
38304833_38318734)
del
GRCh38.p12First PassNC_000011.10Chr1138,227,65638,230,63538,304,83338,318,734
nssv1594894RemappedPerfectNC_000011.10:g.(38
227656_38230635)_(
38304833_38318734)
dup
GRCh38.p12First PassNC_000011.10Chr1138,227,65638,230,63538,304,83338,318,734
nssv1597676RemappedPerfectNC_000011.10:g.(38
227656_38230635)_(
38304833_38318734)
del
GRCh38.p12First PassNC_000011.10Chr1138,227,65638,230,63538,304,83338,318,734
nssv1532048RemappedPerfectNC_000011.9:g.(382
49206_38252185)_(3
8326383_38340284)d
el
GRCh37.p13First PassNC_000011.9Chr1138,249,20638,252,18538,326,38338,340,284
nssv1532157RemappedPerfectNC_000011.9:g.(382
49206_38252185)_(3
8326383_38340284)d
el
GRCh37.p13First PassNC_000011.9Chr1138,249,20638,252,18538,326,38338,340,284
nssv1532680RemappedPerfectNC_000011.9:g.(382
49206_38252185)_(3
8326383_38340284)d
el
GRCh37.p13First PassNC_000011.9Chr1138,249,20638,252,18538,326,38338,340,284
nssv1535583RemappedPerfectNC_000011.9:g.(382
49206_38252185)_(3
8326383_38340284)d
el
GRCh37.p13First PassNC_000011.9Chr1138,249,20638,252,18538,326,38338,340,284
nssv1551347RemappedPerfectNC_000011.9:g.(382
49206_38252185)_(3
8326383_38340284)d
el
GRCh37.p13First PassNC_000011.9Chr1138,249,20638,252,18538,326,38338,340,284
nssv1552859RemappedPerfectNC_000011.9:g.(382
49206_38252185)_(3
8326383_38340284)d
el
GRCh37.p13First PassNC_000011.9Chr1138,249,20638,252,18538,326,38338,340,284
nssv1554634RemappedPerfectNC_000011.9:g.(382
49206_38252185)_(3
8326383_38340284)d
el
GRCh37.p13First PassNC_000011.9Chr1138,249,20638,252,18538,326,38338,340,284
nssv1556349RemappedPerfectNC_000011.9:g.(382
49206_38252185)_(3
8326383_38340284)d
el
GRCh37.p13First PassNC_000011.9Chr1138,249,20638,252,18538,326,38338,340,284
nssv1556630RemappedPerfectNC_000011.9:g.(382
49206_38252185)_(3
8326383_38340284)d
el
GRCh37.p13First PassNC_000011.9Chr1138,249,20638,252,18538,326,38338,340,284
nssv1558996RemappedPerfectNC_000011.9:g.(382
49206_38252185)_(3
8326383_38340284)d
el
GRCh37.p13First PassNC_000011.9Chr1138,249,20638,252,18538,326,38338,340,284
nssv1563971RemappedPerfectNC_000011.9:g.(382
49206_38252185)_(3
8326383_38340284)d
up
GRCh37.p13First PassNC_000011.9Chr1138,249,20638,252,18538,326,38338,340,284
nssv1570135RemappedPerfectNC_000011.9:g.(382
49206_38252185)_(3
8326383_38340284)d
el
GRCh37.p13First PassNC_000011.9Chr1138,249,20638,252,18538,326,38338,340,284
nssv1577773RemappedPerfectNC_000011.9:g.(382
49206_38252185)_(3
8326383_38340284)d
up
GRCh37.p13First PassNC_000011.9Chr1138,249,20638,252,18538,326,38338,340,284
nssv1581850RemappedPerfectNC_000011.9:g.(382
49206_38252185)_(3
8326383_38340284)d
el
GRCh37.p13First PassNC_000011.9Chr1138,249,20638,252,18538,326,38338,340,284
nssv1583065RemappedPerfectNC_000011.9:g.(382
49206_38252185)_(3
8326383_38340284)d
el
GRCh37.p13First PassNC_000011.9Chr1138,249,20638,252,18538,326,38338,340,284
nssv1588661RemappedPerfectNC_000011.9:g.(382
49206_38252185)_(3
8326383_38340284)d
el
GRCh37.p13First PassNC_000011.9Chr1138,249,20638,252,18538,326,38338,340,284
nssv1594894RemappedPerfectNC_000011.9:g.(382
49206_38252185)_(3
8326383_38340284)d
up
GRCh37.p13First PassNC_000011.9Chr1138,249,20638,252,18538,326,38338,340,284
nssv1597676RemappedPerfectNC_000011.9:g.(382
49206_38252185)_(3
8326383_38340284)d
el
GRCh37.p13First PassNC_000011.9Chr1138,249,20638,252,18538,326,38338,340,284
nssv1532048Submitted genomicNC_000011.8:g.(382
05782_38208761)_(3
8282959_38296860)d
el
NCBI36 (hg18)NC_000011.8Chr1138,205,78238,208,76138,282,95938,296,860
nssv1532157Submitted genomicNC_000011.8:g.(382
05782_38208761)_(3
8282959_38296860)d
el
NCBI36 (hg18)NC_000011.8Chr1138,205,78238,208,76138,282,95938,296,860
nssv1532680Submitted genomicNC_000011.8:g.(382
05782_38208761)_(3
8282959_38296860)d
el
NCBI36 (hg18)NC_000011.8Chr1138,205,78238,208,76138,282,95938,296,860
nssv1535583Submitted genomicNC_000011.8:g.(382
05782_38208761)_(3
8282959_38296860)d
el
NCBI36 (hg18)NC_000011.8Chr1138,205,78238,208,76138,282,95938,296,860
nssv1551347Submitted genomicNC_000011.8:g.(382
05782_38208761)_(3
8282959_38296860)d
el
NCBI36 (hg18)NC_000011.8Chr1138,205,78238,208,76138,282,95938,296,860
nssv1552859Submitted genomicNC_000011.8:g.(382
05782_38208761)_(3
8282959_38296860)d
el
NCBI36 (hg18)NC_000011.8Chr1138,205,78238,208,76138,282,95938,296,860
nssv1554634Submitted genomicNC_000011.8:g.(382
05782_38208761)_(3
8282959_38296860)d
el
NCBI36 (hg18)NC_000011.8Chr1138,205,78238,208,76138,282,95938,296,860
nssv1556349Submitted genomicNC_000011.8:g.(382
05782_38208761)_(3
8282959_38296860)d
el
NCBI36 (hg18)NC_000011.8Chr1138,205,78238,208,76138,282,95938,296,860
nssv1556630Submitted genomicNC_000011.8:g.(382
05782_38208761)_(3
8282959_38296860)d
el
NCBI36 (hg18)NC_000011.8Chr1138,205,78238,208,76138,282,95938,296,860
nssv1558996Submitted genomicNC_000011.8:g.(382
05782_38208761)_(3
8282959_38296860)d
el
NCBI36 (hg18)NC_000011.8Chr1138,205,78238,208,76138,282,95938,296,860
nssv1563971Submitted genomicNC_000011.8:g.(382
05782_38208761)_(3
8282959_38296860)d
up
NCBI36 (hg18)NC_000011.8Chr1138,205,78238,208,76138,282,95938,296,860
nssv1570135Submitted genomicNC_000011.8:g.(382
05782_38208761)_(3
8282959_38296860)d
el
NCBI36 (hg18)NC_000011.8Chr1138,205,78238,208,76138,282,95938,296,860
nssv1577773Submitted genomicNC_000011.8:g.(382
05782_38208761)_(3
8282959_38296860)d
up
NCBI36 (hg18)NC_000011.8Chr1138,205,78238,208,76138,282,95938,296,860
nssv1581850Submitted genomicNC_000011.8:g.(382
05782_38208761)_(3
8282959_38296860)d
el
NCBI36 (hg18)NC_000011.8Chr1138,205,78238,208,76138,282,95938,296,860
nssv1583065Submitted genomicNC_000011.8:g.(382
05782_38208761)_(3
8282959_38296860)d
el
NCBI36 (hg18)NC_000011.8Chr1138,205,78238,208,76138,282,95938,296,860
nssv1588661Submitted genomicNC_000011.8:g.(382
05782_38208761)_(3
8282959_38296860)d
el
NCBI36 (hg18)NC_000011.8Chr1138,205,78238,208,76138,282,95938,296,860
nssv1594894Submitted genomicNC_000011.8:g.(382
05782_38208761)_(3
8282959_38296860)d
up
NCBI36 (hg18)NC_000011.8Chr1138,205,78238,208,76138,282,95938,296,860
nssv1597676Submitted genomicNC_000011.8:g.(382
05782_38208761)_(3
8282959_38296860)d
el
NCBI36 (hg18)NC_000011.8Chr1138,205,78238,208,76138,282,95938,296,860

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

Support Center