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nsv6805287

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:121,132

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 371 SVs from 55 studies. See in: genome view    
    Submitted genomic130,713,095-130,834,226Question Mark
    Overlapping variant regions from other studies: 371 SVs from 55 studies. See in: genome view    
    Remapped(Score: Good):131,034,240-131,155,366Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6805287Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr6130,713,095130,834,226
    nsv6805287RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr6131,034,240131,155,366

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18710711duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18710711Submitted genomicNC_000006.12:g.130
    713095_130834226du
    p
    GRCh38 (hg38)NC_000006.12Chr6130,713,095130,834,226
    nssv18710711RemappedGoodNC_000006.11:g.131
    034240_131155366du
    p
    GRCh37.p13First PassNC_000006.11Chr6131,034,240131,155,366

    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)
    nssv187107114e-061273264
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