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nsv6927492

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,753

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 130 SVs from 25 studies. See in: genome view    
    Submitted genomic6,618,176-6,621,928Question Mark
    Overlapping variant regions from other studies: 130 SVs from 25 studies. See in: genome view    
    Remapped(Score: Perfect):6,727,342-6,731,094Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6927492Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr126,618,1766,621,928
    nsv6927492RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr126,727,3426,731,094

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18371366deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18371366Submitted genomicNC_000012.12:g.661
    8176_6621928del
    GRCh38 (hg38)NC_000012.12Chr126,618,1766,621,928
    nssv18371366RemappedPerfectNC_000012.11:g.672
    7342_6731094del
    GRCh37.p13First PassNC_000012.11Chr126,727,3426,731,094

    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)
    nssv183713664e-061276094
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