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nsv6832309

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,011

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 98 SVs from 31 studies. See in: genome view    
    Submitted genomic47,812,700-47,817,710Question Mark
    Overlapping variant regions from other studies: 98 SVs from 31 studies. See in: genome view    
    Remapped(Score: Perfect):47,852,298-47,857,308Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6832309Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr747,812,70047,817,710
    nsv6832309RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr747,852,29847,857,308

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18543266deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18543266Submitted genomicNC_000007.14:g.478
    12700_47817710del
    GRCh38 (hg38)NC_000007.14Chr747,812,70047,817,710
    nssv18543266RemappedPerfectNC_000007.13:g.478
    52298_47857308del
    GRCh37.p13First PassNC_000007.13Chr747,852,29847,857,308

    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)
    nssv185432664e-061276254
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