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nsv6645699

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:186

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 163 SVs from 25 studies. See in: genome view    
    Submitted genomic180,475,045-180,475,230Question Mark
    Overlapping variant regions from other studies: 165 SVs from 25 studies. See in: genome view    
    Remapped(Score: Perfect):180,444,180-180,444,365Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6645699Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1180,475,045180,475,230
    nsv6645699RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1180,444,180180,444,365

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18572447duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18572447Submitted genomicNC_000001.11:g.180
    475045_180475230du
    p
    GRCh38 (hg38)NC_000001.11Chr1180,475,045180,475,230
    nssv18572447RemappedPerfectNC_000001.10:g.180
    444180_180444365du
    p
    GRCh37.p13First PassNC_000001.10Chr1180,444,180180,444,365

    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)
    nssv18572447<0.00126233294
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