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nsv2745430

  • Variant Calls:2
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:10,456,499

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 2555 SVs from 90 studies. See in: genome view    
Remapped(Score: Pass):36,010,041-46,466,539Question Mark
Overlapping variant regions from other studies: 3014 SVs from 81 studies. See in: genome view    
Remapped(Score: Pass):35,244,412-46,500,451Question Mark
Overlapping variant regions from other studies: 1038 SVs from 24 studies. See in: genome view    
Submitted genomic35,101,913-45,057,952Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nsv2745430RemappedPassGRCh38.p12Primary AssemblyFirst PassNC_000016.10Chr1636,010,04146,466,539
nsv2745430RemappedPassGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr1635,244,41246,500,451
nsv2745430Submitted genomicNCBI36 (hg18)Primary AssemblyNC_000016.8Chr1635,101,91345,057,952

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv13555440deletionSNP arrayProbe signal intensity
nssv13566271deletionSNP arrayProbe signal intensity

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
nssv13555440RemappedPassNC_000016.10:g.(?_
36010041)_(4646653
9_?)del
GRCh38.p12First PassNC_000016.10Chr1636,010,04146,466,539
nssv13566271RemappedPassNC_000016.10:g.(?_
36010041)_(4646653
9_?)del
GRCh38.p12First PassNC_000016.10Chr1636,010,04146,466,539
nssv13555440RemappedPassNC_000016.9:g.(?_3
5244412)_(46500451
_?)del
GRCh37.p13First PassNC_000016.9Chr1635,244,41246,500,451
nssv13566271RemappedPassNC_000016.9:g.(?_3
5244412)_(46500451
_?)del
GRCh37.p13First PassNC_000016.9Chr1635,244,41246,500,451
nssv13555440Submitted genomicNC_000016.8:g.(?_3
5101913)_(45057952
_?)del
NCBI36 (hg18)NC_000016.8Chr1635,101,91345,057,952
nssv13566271Submitted genomicNC_000016.8:g.(?_3
5101913)_(45057952
_?)del
NCBI36 (hg18)NC_000016.8Chr1635,101,91345,057,952

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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