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nsv6786838

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:126

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 78 SVs from 16 studies. See in: genome view    
    Submitted genomic41,249,025-41,249,150Question Mark
    Overlapping variant regions from other studies: 78 SVs from 16 studies. See in: genome view    
    Remapped(Score: Perfect):41,216,763-41,216,888Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6786838Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr641,249,02541,249,150
    nsv6786838RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr641,216,76341,216,888

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18715461duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18715461Submitted genomicNC_000006.12:g.412
    49025_41249150dup
    GRCh38 (hg38)NC_000006.12Chr641,249,02541,249,150
    nssv18715461RemappedPerfectNC_000006.11:g.412
    16763_41216888dup
    GRCh37.p13First PassNC_000006.11Chr641,216,76341,216,888

    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)
    nssv187154614e-061228418
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