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nsv7013447

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:7,417

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 96 SVs from 34 studies. See in: genome view    
    Submitted genomic57,195,542-57,202,958Question Mark
    Overlapping variant regions from other studies: 96 SVs from 34 studies. See in: genome view    
    Remapped(Score: Perfect):57,706,910-57,714,326Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7013447Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1957,195,54257,202,958
    nsv7013447RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1957,706,91057,714,326

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18426910deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18426910Submitted genomicNC_000019.10:g.571
    95542_57202958del
    GRCh38 (hg38)NC_000019.10Chr1957,195,54257,202,958
    nssv18426910RemappedPerfectNC_000019.9:g.5770
    6910_57714326del
    GRCh37.p13First PassNC_000019.9Chr1957,706,91057,714,326

    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)
    nssv184269100.012812276060
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