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nsv6832418

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:43

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 101 SVs from 22 studies. See in: genome view    
    Submitted genomic138,572,462-138,572,504Question Mark
    Overlapping variant regions from other studies: 101 SVs from 22 studies. See in: genome view    
    Remapped(Score: Perfect):138,257,207-138,257,249Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6832418Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr7138,572,462138,572,504
    nsv6832418RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr7138,257,207138,257,249

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18538393deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18538393Submitted genomicNC_000007.14:g.138
    572462_138572504de
    l
    GRCh38 (hg38)NC_000007.14Chr7138,572,462138,572,504
    nssv18538393RemappedPerfectNC_000007.13:g.138
    257207_138257249de
    l
    GRCh37.p13First PassNC_000007.13Chr7138,257,207138,257,249

    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)
    nssv185383930.444113764256322
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