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nsv6262855

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:85

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 116 SVs from 28 studies. See in: genome view    
Submitted genomic141,771,409-141,771,493Question Mark
Overlapping variant regions from other studies: 116 SVs from 28 studies. See in: genome view    
Remapped(Score: Perfect):141,490,251-141,490,335Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv6262855Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3141,771,409141,771,493
nsv6262855RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3141,490,251141,490,335

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17868133deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17868133Submitted genomicNC_000003.12:g.141
771409_141771493de
l
GRCh38 (hg38)NC_000003.12Chr3141,771,409141,771,493
nssv17868133RemappedPerfectNC_000003.11:g.141
490251_141490335de
l
GRCh37.p13First PassNC_000003.11Chr3141,490,251141,490,335

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)
nssv178681330.0651482272
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