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nsv6816810

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:7,010

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 170 SVs from 31 studies. See in: genome view    
    Submitted genomic2,405,005-2,412,014Question Mark
    Overlapping variant regions from other studies: 170 SVs from 31 studies. See in: genome view    
    Remapped(Score: Perfect):2,444,640-2,451,649Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6816810Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr72,405,0052,412,014
    nsv6816810RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr72,444,6402,451,649

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18540119deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18540119Submitted genomicNC_000007.14:g.240
    5005_2412014del
    GRCh38 (hg38)NC_000007.14Chr72,405,0052,412,014
    nssv18540119RemappedPerfectNC_000007.13:g.244
    4640_2451649del
    GRCh37.p13First PassNC_000007.13Chr72,444,6402,451,649

    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)
    nssv185401191.1e-053275154
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