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nsv6261507

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:119

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 132 SVs from 34 studies. See in: genome view    
Submitted genomic118,094,248-118,094,366Question Mark
Overlapping variant regions from other studies: 132 SVs from 34 studies. See in: genome view    
Remapped(Score: Perfect):118,851,824-118,851,942Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv6261507Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2118,094,248118,094,366
nsv6261507RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2118,851,824118,851,942

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17876798deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17876798Submitted genomicNC_000002.12:g.118
094248_118094366de
l
GRCh38 (hg38)NC_000002.12Chr2118,094,248118,094,366
nssv17876798RemappedPerfectNC_000002.11:g.118
851824_118851942de
l
GRCh37.p13First PassNC_000002.11Chr2118,851,824118,851,942

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

Genotype Information

Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
nssv178767980.00242300
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