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nsv8926

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:19,850

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 103 SVs from 14 studies. See in: genome view    
Remapped(Score: Perfect):18,391,169-18,411,018Question Mark
Overlapping variant regions from other studies: 104 SVs from 14 studies. See in: genome view    
Remapped(Score: Perfect):18,544,103-18,563,952Question Mark
Submitted genomic18,435,370-18,455,219Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartOuter Stop
nsv8926RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000012.12Chr1218,391,16918,411,018
nsv8926RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1218,544,10318,563,952
nsv8926Submitted genomicNCBI35 (hg17)Primary AssemblyNC_000012.9Chr1218,435,37018,455,219

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv19072copy number lossNA18942Oligo aCGHProbe signal intensity504

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
nssv19072RemappedPerfectNC_000012.12:g.(18
391169_18406824)_(
18407388_18411018)
del
GRCh38.p12First PassNC_000012.12Chr1218,391,16918,406,82418,407,38818,411,018
nssv19072RemappedPerfectNC_000012.11:g.(18
544103_18559758)_(
18560322_18563952)
del
GRCh37.p13First PassNC_000012.11Chr1218,544,10318,559,75818,560,32218,563,952
nssv19072Submitted genomicNC_000012.9:g.(184
35370_18451025)_(1
8451589_18455219)d
el
NCBI35 (hg17)NC_000012.9Chr1218,435,37018,451,02518,451,58918,455,219

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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