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nsv6855586

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:77

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 253 SVs from 36 studies. See in: genome view    
    Submitted genomic11,379,843-11,379,919Question Mark
    Overlapping variant regions from other studies: 253 SVs from 36 studies. See in: genome view    
    Remapped(Score: Perfect):11,237,352-11,237,428Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6855586Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr811,379,84311,379,919
    nsv6855586RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr811,237,35211,237,428

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18548512deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18548512Submitted genomicNC_000008.11:g.113
    79843_11379919del
    GRCh38 (hg38)NC_000008.11Chr811,379,84311,379,919
    nssv18548512RemappedPerfectNC_000008.10:g.112
    37352_11237428del
    GRCh37.p13First PassNC_000008.10Chr811,237,35211,237,428

    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)
    nssv185485121.6e-054250678
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