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nsv6602908

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:381

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 95 SVs from 33 studies. See in: genome view    
    Submitted genomic45,736,215-45,736,595Question Mark
    Overlapping variant regions from other studies: 95 SVs from 33 studies. See in: genome view    
    Remapped(Score: Perfect):45,775,814-45,776,194Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6602908Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr745,736,21545,736,595
    nsv6602908RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr745,775,81445,776,194

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18155078deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18155078Submitted genomicNC_000007.14:g.457
    36215_45736595del
    GRCh38 (hg38)NC_000007.14Chr745,736,21545,736,595
    nssv18155078RemappedPerfectNC_000007.13:g.457
    75814_45776194del
    GRCh37.p13First PassNC_000007.13Chr745,775,81445,776,194

    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)
    nssv181550780.216783736252
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