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nsv6713870

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:133,923

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 508 SVs from 59 studies. See in: genome view    
    Submitted genomic121,430,965-121,564,887Question Mark
    Overlapping variant regions from other studies: 508 SVs from 59 studies. See in: genome view    
    Remapped(Score: Perfect):121,149,812-121,283,734Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6713870Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3121,430,965121,564,887
    nsv6713870RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3121,149,812121,283,734

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18471910deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18471910Submitted genomicNC_000003.12:g.121
    430965_121564887de
    l
    GRCh38 (hg38)NC_000003.12Chr3121,430,965121,564,887
    nssv18471910RemappedPerfectNC_000003.11:g.121
    149812_121283734de
    l
    GRCh37.p13First PassNC_000003.11Chr3121,149,812121,283,734

    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)
    nssv184719105.3e-0515275948
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