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nsv6949750

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:111,898

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 301 SVs from 42 studies. See in: genome view    
    Submitted genomic60,941,772-61,053,669Question Mark
    Overlapping variant regions from other studies: 301 SVs from 42 studies. See in: genome view    
    Remapped(Score: Perfect):61,408,490-61,520,387Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6949750Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000014.9Chr1460,941,77261,053,669
    nsv6949750RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000014.8Chr1461,408,49061,520,387

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18617166duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18617166Submitted genomicNC_000014.9:g.6094
    1772_61053669dup
    GRCh38 (hg38)NC_000014.9Chr1460,941,77261,053,669
    nssv18617166RemappedPerfectNC_000014.8:g.6140
    8490_61520387dup
    GRCh37.p13First PassNC_000014.8Chr1461,408,49061,520,387

    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)
    nssv186171664e-061274984
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