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nsv6787758

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:15,937

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 810 SVs from 76 studies. See in: genome view    
    Submitted genomic31,338,160-31,354,096Question Mark
    Overlapping variant regions from other studies: 810 SVs from 76 studies. See in: genome view    
    Remapped(Score: Perfect):31,305,937-31,321,873Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6787758Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr631,338,16031,354,096
    nsv6787758RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr631,305,93731,321,873

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18525224deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18525224Submitted genomicNC_000006.12:g.313
    38160_31354096del
    GRCh38 (hg38)NC_000006.12Chr631,338,16031,354,096
    nssv18525224RemappedPerfectNC_000006.11:g.313
    05937_31321873del
    GRCh37.p13First PassNC_000006.11Chr631,305,93731,321,873

    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)
    nssv185252244e-061276242
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