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nsv6785872

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:36,642

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 238 SVs from 47 studies. See in: genome view    
    Submitted genomic27,795,474-27,832,115Question Mark
    Overlapping variant regions from other studies: 238 SVs from 47 studies. See in: genome view    
    Remapped(Score: Good):27,763,253-27,799,893Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6785872Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr627,795,47427,832,115
    nsv6785872RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr627,763,25327,799,893

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18714760duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18714760Submitted genomicNC_000006.12:g.277
    95474_27832115dup
    GRCh38 (hg38)NC_000006.12Chr627,795,47427,832,115
    nssv18714760RemappedGoodNC_000006.11:g.277
    63253_27799893dup
    GRCh37.p13First PassNC_000006.11Chr627,763,25327,799,893

    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)
    nssv187147604e-061275472
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