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nsv6773609

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,500

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 111 SVs from 19 studies. See in: genome view    
    Submitted genomic124,395,201-124,399,700Question Mark
    Overlapping variant regions from other studies: 111 SVs from 19 studies. See in: genome view    
    Remapped(Score: Perfect):123,730,894-123,735,393Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6773609Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5124,395,201124,399,700
    nsv6773609RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5123,730,894123,735,393

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18693916duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18693916Submitted genomicNC_000005.10:g.124
    395201_124399700du
    p
    GRCh38 (hg38)NC_000005.10Chr5124,395,201124,399,700
    nssv18693916RemappedPerfectNC_000005.9:g.1237
    30894_123735393dup
    GRCh37.p13First PassNC_000005.9Chr5123,730,894123,735,393

    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)
    nssv186939164e-061274796
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