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nsv6734344

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:42,299

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 563 SVs from 70 studies. See in: genome view    
    Submitted genomic6,646,532-6,688,830Question Mark
    Overlapping variant regions from other studies: 563 SVs from 70 studies. See in: genome view    
    Remapped(Score: Perfect):6,648,259-6,690,557Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6734344Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr46,646,5326,688,830
    nsv6734344RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr46,648,2596,690,557

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18500028deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18500028Submitted genomicNC_000004.12:g.664
    6532_6688830del
    GRCh38 (hg38)NC_000004.12Chr46,646,5326,688,830
    nssv18500028RemappedPerfectNC_000004.11:g.664
    8259_6690557del
    GRCh37.p13First PassNC_000004.11Chr46,648,2596,690,557

    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)
    nssv185000284e-061276156
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