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nsv6778396

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,254,497

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 5832 SVs from 97 studies. See in: genome view    
    Submitted genomic13,240,748-15,495,244Question Mark
    Overlapping variant regions from other studies: 5832 SVs from 97 studies. See in: genome view    
    Remapped(Score: Perfect):13,240,980-15,495,475Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6778396Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr613,240,74815,495,244
    nsv6778396RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr613,240,98015,495,475

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18710285duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18710285Submitted genomicNC_000006.12:g.132
    40748_15495244dup
    GRCh38 (hg38)NC_000006.12Chr613,240,74815,495,244
    nssv18710285RemappedPerfectNC_000006.11:g.132
    40980_15495475dup
    GRCh37.p13First PassNC_000006.11Chr613,240,98015,495,475

    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)
    nssv187102854e-061275970
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