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nsv7001942

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,100

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 105 SVs from 32 studies. See in: genome view    
    Submitted genomic53,269,601-53,270,700Question Mark
    Overlapping variant regions from other studies: 105 SVs from 32 studies. See in: genome view    
    Remapped(Score: Perfect):53,772,854-53,773,953Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7001942Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1953,269,60153,270,700
    nsv7001942RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1953,772,85453,773,953

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18426123deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18426123Submitted genomicNC_000019.10:g.532
    69601_53270700del
    GRCh38 (hg38)NC_000019.10Chr1953,269,60153,270,700
    nssv18426123RemappedPerfectNC_000019.9:g.5377
    2854_53773953del
    GRCh37.p13First PassNC_000019.9Chr1953,772,85453,773,953

    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)
    nssv184261230.04410422242748
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