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nsv6970371

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:363,899

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 877 SVs from 65 studies. See in: genome view    
    Submitted genomic59,749,824-60,113,722Question Mark
    Overlapping variant regions from other studies: 877 SVs from 65 studies. See in: genome view    
    Remapped(Score: Perfect):60,042,023-60,405,921Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6970371Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1559,749,82460,113,722
    nsv6970371RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1560,042,02360,405,921

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18620298duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18620298Submitted genomicNC_000015.10:g.597
    49824_60113722dup
    GRCh38 (hg38)NC_000015.10Chr1559,749,82460,113,722
    nssv18620298RemappedPerfectNC_000015.9:g.6004
    2023_60405921dup
    GRCh37.p13First PassNC_000015.9Chr1560,042,02360,405,921

    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)
    nssv186202984e-061272698
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