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nsv6992943

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,028

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 110 SVs from 12 studies. See in: genome view    
    Submitted genomic78,063,965-78,064,992Question Mark
    Overlapping variant regions from other studies: 110 SVs from 12 studies. See in: genome view    
    Remapped(Score: Perfect):76,060,046-76,061,073Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6992943Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1778,063,96578,064,992
    nsv6992943RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1776,060,04676,061,073

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18631414duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18631414Submitted genomicNC_000017.11:g.780
    63965_78064992dup
    GRCh38 (hg38)NC_000017.11Chr1778,063,96578,064,992
    nssv18631414RemappedPerfectNC_000017.10:g.760
    60046_76061073dup
    GRCh37.p13First PassNC_000017.10Chr1776,060,04676,061,073

    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)
    nssv186314144e-061253456
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