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nsv6289775

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

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 108 SVs from 25 studies. See in: genome view    
Submitted genomic125,307,740-125,307,740Question Mark
Overlapping variant regions from other studies: 108 SVs from 25 studies. See in: genome view    
Remapped(Score: Perfect):125,792,286-125,792,286Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv6289775Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr12125,307,740125,307,740
nsv6289775RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr12125,792,286125,792,286

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17931021insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17931021Submitted genomicNC_000012.12:g.125
307740_125307741in
s74
GRCh38 (hg38)NC_000012.12Chr12125,307,740125,307,740
nssv17931021RemappedPerfectNC_000012.11:g.125
792286_125792287in
s74
GRCh37.p13First PassNC_000012.11Chr12125,792,286125,792,286

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)
nssv179310210.00242166
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