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nsv6823386

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:61

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 123 SVs from 41 studies. See in: genome view    
    Submitted genomic32,762,337-32,762,397Question Mark
    Overlapping variant regions from other studies: 123 SVs from 41 studies. See in: genome view    
    Remapped(Score: Perfect):32,801,949-32,802,009Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6823386Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr732,762,33732,762,397
    nsv6823386RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr732,801,94932,802,009

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18540446deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18540446Submitted genomicNC_000007.14:g.327
    62337_32762397del
    GRCh38 (hg38)NC_000007.14Chr732,762,33732,762,397
    nssv18540446RemappedPerfectNC_000007.13:g.328
    01949_32802009del
    GRCh37.p13First PassNC_000007.13Chr732,801,94932,802,009

    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)
    nssv185404460.15238537253808
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