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nsv6532775

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:6,798

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 152 SVs from 38 studies. See in: genome view    
    Submitted genomic49,947,140-49,953,937Question Mark
    Overlapping variant regions from other studies: 152 SVs from 38 studies. See in: genome view    
    Remapped(Score: Perfect):50,450,397-50,457,194Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6532775Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1949,947,14049,953,937
    nsv6532775RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1950,450,39750,457,194

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18049066deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18049066Submitted genomicNC_000019.10:g.499
    47140_49953937del
    GRCh38 (hg38)NC_000019.10Chr1949,947,14049,953,937
    nssv18049066RemappedPerfectNC_000019.9:g.5045
    0397_50457194del
    GRCh37.p13First PassNC_000019.9Chr1950,450,39750,457,194

    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)
    nssv18049066<0.001839102
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