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nsv6832530

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,570

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 135 SVs from 35 studies. See in: genome view    
    Submitted genomic137,553,444-137,558,013Question Mark
    Overlapping variant regions from other studies: 135 SVs from 35 studies. See in: genome view    
    Remapped(Score: Perfect):137,238,190-137,242,759Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6832530Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr7137,553,444137,558,013
    nsv6832530RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr7137,238,190137,242,759

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18538291deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18538291Submitted genomicNC_000007.14:g.137
    553444_137558013de
    l
    GRCh38 (hg38)NC_000007.14Chr7137,553,444137,558,013
    nssv18538291RemappedPerfectNC_000007.13:g.137
    238190_137242759de
    l
    GRCh37.p13First PassNC_000007.13Chr7137,238,190137,242,759

    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)
    nssv185382911.8e-055275802
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