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nsv881970

  • Variant Calls:16
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:75,580

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 598 SVs from 59 studies. See in: genome view    
Remapped(Score: Perfect):70,381,705-70,457,284Question Mark
Overlapping variant regions from other studies: 598 SVs from 59 studies. See in: genome view    
Remapped(Score: Perfect):69,677,532-69,753,111Question Mark
Overlapping variant regions from other studies: 368 SVs from 21 studies. See in: genome view    
Submitted genomic69,713,288-69,788,867Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
nsv881970RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000005.10Chr570,381,70570,392,52370,441,47270,457,284
nsv881970RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr569,677,53269,688,35069,737,29969,753,111
nsv881970Submitted genomicNCBI36 (hg18)Primary AssemblyNC_000005.8Chr569,713,28869,724,10669,773,05569,788,867

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv1527273copy number gainSP58310SNP arraySNP genotyping analysis14
nssv1534060copy number gainMS11444SNP arraySNP genotyping analysis10
nssv1540193copy number gainMS14728SNP arraySNP genotyping analysis13
nssv1542666copy number gainMS15826SNP arraySNP genotyping analysis14
nssv1546005copy number gainMS17097SNP arraySNP genotyping analysis13
nssv1546354copy number gainMS17158SNP arraySNP genotyping analysis10
nssv1547616copy number gainMS17492SNP arraySNP genotyping analysis17
nssv1550274copy number gainMS18387SNP arraySNP genotyping analysis20
nssv1551657copy number gainMS18966SNP arraySNP genotyping analysis9
nssv1552456copy number gainMS19437SNP arraySNP genotyping analysis18
nssv1554195copy number gainMS20640SNP arraySNP genotyping analysis9
nssv1561678copy number gainMS25181SNP arraySNP genotyping analysis10
nssv1566681copy number gainIS30837SNP arraySNP genotyping analysis21
nssv1579552copy number gainIS35129SNP arraySNP genotyping analysis12
nssv1596422copy number gainIS40503SNP arraySNP genotyping analysis12
nssv1599238copy number gainIS41483SNP arraySNP genotyping analysis10

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
nssv1527273RemappedPerfectNC_000005.10:g.(70
381705_70392523)_(
70441472_70457284)
dup
GRCh38.p12First PassNC_000005.10Chr570,381,70570,392,52370,441,47270,457,284
nssv1534060RemappedPerfectNC_000005.10:g.(70
381705_70392523)_(
70441472_70457284)
dup
GRCh38.p12First PassNC_000005.10Chr570,381,70570,392,52370,441,47270,457,284
nssv1540193RemappedPerfectNC_000005.10:g.(70
381705_70392523)_(
70441472_70457284)
dup
GRCh38.p12First PassNC_000005.10Chr570,381,70570,392,52370,441,47270,457,284
nssv1542666RemappedPerfectNC_000005.10:g.(70
381705_70392523)_(
70441472_70457284)
dup
GRCh38.p12First PassNC_000005.10Chr570,381,70570,392,52370,441,47270,457,284
nssv1546005RemappedPerfectNC_000005.10:g.(70
381705_70392523)_(
70441472_70457284)
dup
GRCh38.p12First PassNC_000005.10Chr570,381,70570,392,52370,441,47270,457,284
nssv1546354RemappedPerfectNC_000005.10:g.(70
381705_70392523)_(
70441472_70457284)
dup
GRCh38.p12First PassNC_000005.10Chr570,381,70570,392,52370,441,47270,457,284
nssv1547616RemappedPerfectNC_000005.10:g.(70
381705_70392523)_(
70441472_70457284)
dup
GRCh38.p12First PassNC_000005.10Chr570,381,70570,392,52370,441,47270,457,284
nssv1550274RemappedPerfectNC_000005.10:g.(70
381705_70392523)_(
70441472_70457284)
dup
GRCh38.p12First PassNC_000005.10Chr570,381,70570,392,52370,441,47270,457,284
nssv1551657RemappedPerfectNC_000005.10:g.(70
381705_70392523)_(
70441472_70457284)
dup
GRCh38.p12First PassNC_000005.10Chr570,381,70570,392,52370,441,47270,457,284
nssv1552456RemappedPerfectNC_000005.10:g.(70
381705_70392523)_(
70441472_70457284)
dup
GRCh38.p12First PassNC_000005.10Chr570,381,70570,392,52370,441,47270,457,284
nssv1554195RemappedPerfectNC_000005.10:g.(70
381705_70392523)_(
70441472_70457284)
dup
GRCh38.p12First PassNC_000005.10Chr570,381,70570,392,52370,441,47270,457,284
nssv1561678RemappedPerfectNC_000005.10:g.(70
381705_70392523)_(
70441472_70457284)
dup
GRCh38.p12First PassNC_000005.10Chr570,381,70570,392,52370,441,47270,457,284
nssv1566681RemappedPerfectNC_000005.10:g.(70
381705_70392523)_(
70441472_70457284)
dup
GRCh38.p12First PassNC_000005.10Chr570,381,70570,392,52370,441,47270,457,284
nssv1579552RemappedPerfectNC_000005.10:g.(70
381705_70392523)_(
70441472_70457284)
dup
GRCh38.p12First PassNC_000005.10Chr570,381,70570,392,52370,441,47270,457,284
nssv1596422RemappedPerfectNC_000005.10:g.(70
381705_70392523)_(
70441472_70457284)
dup
GRCh38.p12First PassNC_000005.10Chr570,381,70570,392,52370,441,47270,457,284
nssv1599238RemappedPerfectNC_000005.10:g.(70
381705_70392523)_(
70441472_70457284)
dup
GRCh38.p12First PassNC_000005.10Chr570,381,70570,392,52370,441,47270,457,284
nssv1527273RemappedPerfectNC_000005.9:g.(696
77532_69688350)_(6
9737299_69753111)d
up
GRCh37.p13First PassNC_000005.9Chr569,677,53269,688,35069,737,29969,753,111
nssv1534060RemappedPerfectNC_000005.9:g.(696
77532_69688350)_(6
9737299_69753111)d
up
GRCh37.p13First PassNC_000005.9Chr569,677,53269,688,35069,737,29969,753,111
nssv1540193RemappedPerfectNC_000005.9:g.(696
77532_69688350)_(6
9737299_69753111)d
up
GRCh37.p13First PassNC_000005.9Chr569,677,53269,688,35069,737,29969,753,111
nssv1542666RemappedPerfectNC_000005.9:g.(696
77532_69688350)_(6
9737299_69753111)d
up
GRCh37.p13First PassNC_000005.9Chr569,677,53269,688,35069,737,29969,753,111
nssv1546005RemappedPerfectNC_000005.9:g.(696
77532_69688350)_(6
9737299_69753111)d
up
GRCh37.p13First PassNC_000005.9Chr569,677,53269,688,35069,737,29969,753,111
nssv1546354RemappedPerfectNC_000005.9:g.(696
77532_69688350)_(6
9737299_69753111)d
up
GRCh37.p13First PassNC_000005.9Chr569,677,53269,688,35069,737,29969,753,111
nssv1547616RemappedPerfectNC_000005.9:g.(696
77532_69688350)_(6
9737299_69753111)d
up
GRCh37.p13First PassNC_000005.9Chr569,677,53269,688,35069,737,29969,753,111
nssv1550274RemappedPerfectNC_000005.9:g.(696
77532_69688350)_(6
9737299_69753111)d
up
GRCh37.p13First PassNC_000005.9Chr569,677,53269,688,35069,737,29969,753,111
nssv1551657RemappedPerfectNC_000005.9:g.(696
77532_69688350)_(6
9737299_69753111)d
up
GRCh37.p13First PassNC_000005.9Chr569,677,53269,688,35069,737,29969,753,111
nssv1552456RemappedPerfectNC_000005.9:g.(696
77532_69688350)_(6
9737299_69753111)d
up
GRCh37.p13First PassNC_000005.9Chr569,677,53269,688,35069,737,29969,753,111
nssv1554195RemappedPerfectNC_000005.9:g.(696
77532_69688350)_(6
9737299_69753111)d
up
GRCh37.p13First PassNC_000005.9Chr569,677,53269,688,35069,737,29969,753,111
nssv1561678RemappedPerfectNC_000005.9:g.(696
77532_69688350)_(6
9737299_69753111)d
up
GRCh37.p13First PassNC_000005.9Chr569,677,53269,688,35069,737,29969,753,111
nssv1566681RemappedPerfectNC_000005.9:g.(696
77532_69688350)_(6
9737299_69753111)d
up
GRCh37.p13First PassNC_000005.9Chr569,677,53269,688,35069,737,29969,753,111
nssv1579552RemappedPerfectNC_000005.9:g.(696
77532_69688350)_(6
9737299_69753111)d
up
GRCh37.p13First PassNC_000005.9Chr569,677,53269,688,35069,737,29969,753,111
nssv1596422RemappedPerfectNC_000005.9:g.(696
77532_69688350)_(6
9737299_69753111)d
up
GRCh37.p13First PassNC_000005.9Chr569,677,53269,688,35069,737,29969,753,111
nssv1599238RemappedPerfectNC_000005.9:g.(696
77532_69688350)_(6
9737299_69753111)d
up
GRCh37.p13First PassNC_000005.9Chr569,677,53269,688,35069,737,29969,753,111
nssv1527273Submitted genomicNC_000005.8:g.(697
13288_69724106)_(6
9773055_69788867)d
up
NCBI36 (hg18)NC_000005.8Chr569,713,28869,724,10669,773,05569,788,867
nssv1534060Submitted genomicNC_000005.8:g.(697
13288_69724106)_(6
9773055_69788867)d
up
NCBI36 (hg18)NC_000005.8Chr569,713,28869,724,10669,773,05569,788,867
nssv1540193Submitted genomicNC_000005.8:g.(697
13288_69724106)_(6
9773055_69788867)d
up
NCBI36 (hg18)NC_000005.8Chr569,713,28869,724,10669,773,05569,788,867
nssv1542666Submitted genomicNC_000005.8:g.(697
13288_69724106)_(6
9773055_69788867)d
up
NCBI36 (hg18)NC_000005.8Chr569,713,28869,724,10669,773,05569,788,867
nssv1546005Submitted genomicNC_000005.8:g.(697
13288_69724106)_(6
9773055_69788867)d
up
NCBI36 (hg18)NC_000005.8Chr569,713,28869,724,10669,773,05569,788,867
nssv1546354Submitted genomicNC_000005.8:g.(697
13288_69724106)_(6
9773055_69788867)d
up
NCBI36 (hg18)NC_000005.8Chr569,713,28869,724,10669,773,05569,788,867
nssv1547616Submitted genomicNC_000005.8:g.(697
13288_69724106)_(6
9773055_69788867)d
up
NCBI36 (hg18)NC_000005.8Chr569,713,28869,724,10669,773,05569,788,867
nssv1550274Submitted genomicNC_000005.8:g.(697
13288_69724106)_(6
9773055_69788867)d
up
NCBI36 (hg18)NC_000005.8Chr569,713,28869,724,10669,773,05569,788,867
nssv1551657Submitted genomicNC_000005.8:g.(697
13288_69724106)_(6
9773055_69788867)d
up
NCBI36 (hg18)NC_000005.8Chr569,713,28869,724,10669,773,05569,788,867
nssv1552456Submitted genomicNC_000005.8:g.(697
13288_69724106)_(6
9773055_69788867)d
up
NCBI36 (hg18)NC_000005.8Chr569,713,28869,724,10669,773,05569,788,867
nssv1554195Submitted genomicNC_000005.8:g.(697
13288_69724106)_(6
9773055_69788867)d
up
NCBI36 (hg18)NC_000005.8Chr569,713,28869,724,10669,773,05569,788,867
nssv1561678Submitted genomicNC_000005.8:g.(697
13288_69724106)_(6
9773055_69788867)d
up
NCBI36 (hg18)NC_000005.8Chr569,713,28869,724,10669,773,05569,788,867
nssv1566681Submitted genomicNC_000005.8:g.(697
13288_69724106)_(6
9773055_69788867)d
up
NCBI36 (hg18)NC_000005.8Chr569,713,28869,724,10669,773,05569,788,867
nssv1579552Submitted genomicNC_000005.8:g.(697
13288_69724106)_(6
9773055_69788867)d
up
NCBI36 (hg18)NC_000005.8Chr569,713,28869,724,10669,773,05569,788,867
nssv1596422Submitted genomicNC_000005.8:g.(697
13288_69724106)_(6
9773055_69788867)d
up
NCBI36 (hg18)NC_000005.8Chr569,713,28869,724,10669,773,05569,788,867
nssv1599238Submitted genomicNC_000005.8:g.(697
13288_69724106)_(6
9773055_69788867)d
up
NCBI36 (hg18)NC_000005.8Chr569,713,28869,724,10669,773,05569,788,867

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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