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nsv6786779

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:563

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 175 SVs from 34 studies. See in: genome view    
    Submitted genomic3,195,159-3,195,721Question Mark
    Overlapping variant regions from other studies: 175 SVs from 34 studies. See in: genome view    
    Remapped(Score: Perfect):3,195,393-3,195,955Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6786779Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr63,195,1593,195,721
    nsv6786779RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr63,195,3933,195,955

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18527925deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18527925Submitted genomicNC_000006.12:g.319
    5159_3195721del
    GRCh38 (hg38)NC_000006.12Chr63,195,1593,195,721
    nssv18527925RemappedPerfectNC_000006.11:g.319
    5393_3195955del
    GRCh37.p13First PassNC_000006.11Chr63,195,3933,195,955

    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)
    nssv185279250.05614827269646
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