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nsv6408695

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:15,474

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 197 SVs from 45 studies. See in: genome view    
    Submitted genomic30,801,388-30,816,861Question Mark
    Overlapping variant regions from other studies: 197 SVs from 45 studies. See in: genome view    
    Remapped(Score: Perfect):30,769,165-30,784,638Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6408695Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr630,801,38830,816,861
    nsv6408695RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr630,769,16530,784,638

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18141456deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18141456Submitted genomicNC_000006.12:g.308
    01388_30816861del
    GRCh38 (hg38)NC_000006.12Chr630,801,38830,816,861
    nssv18141456RemappedPerfectNC_000006.11:g.307
    69165_30784638del
    GRCh37.p13First PassNC_000006.11Chr630,769,16530,784,638

    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)
    nssv18141456<0.001139148
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