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nsv482846

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:167,686

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 535 SVs from 59 studies. See in: genome view    
Remapped(Score: Perfect):101,896,701-102,064,386Question Mark
Overlapping variant regions from other studies: 533 SVs from 59 studies. See in: genome view    
Remapped(Score: Perfect):101,539,981-101,707,666Question Mark
Submitted genomic101,100,162-101,267,847Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nsv482846RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000007.14Chr7101,896,701102,064,386
nsv482846RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr7101,539,981101,707,666
nsv482846Submitted genomicNCBI34 (hg16)Primary AssemblyNC_000007.10Chr7101,100,162101,267,847

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv3007553copy number lossBAC aCGHProbe signal intensity

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
nssv3007553RemappedPerfectNC_000007.14:g.(?_
101896701)_(102064
386_?)del
GRCh38.p12First PassNC_000007.14Chr7101,896,701102,064,386
nssv3007553RemappedPerfectNC_000007.13:g.(?_
101539981)_(101707
666_?)del
GRCh37.p13First PassNC_000007.13Chr7101,539,981101,707,666
nssv3007553Submitted genomicNC_000007.10:g.(?_
101100162)_(101267
847_?)del
NCBI34 (hg16)NC_000007.10Chr7101,100,162101,267,847

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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