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nsv6995737

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:147

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 134 SVs from 28 studies. See in: genome view    
    Submitted genomic62,729,923-62,730,069Question Mark
    Overlapping variant regions from other studies: 134 SVs from 28 studies. See in: genome view    
    Remapped(Score: Perfect):60,807,284-60,807,430Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6995737Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1762,729,92362,730,069
    nsv6995737RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1760,807,28460,807,430

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18628127duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18628127Submitted genomicNC_000017.11:g.627
    29923_62730069dup
    GRCh38 (hg38)NC_000017.11Chr1762,729,92362,730,069
    nssv18628127RemappedPerfectNC_000017.10:g.608
    07284_60807430dup
    GRCh37.p13First PassNC_000017.10Chr1760,807,28460,807,430

    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)
    nssv186281270.21344811208768
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