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nsv6645730

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,300

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 151 SVs from 21 studies. See in: genome view    
    Submitted genomic179,684,101-179,689,400Question Mark
    Overlapping variant regions from other studies: 153 SVs from 21 studies. See in: genome view    
    Remapped(Score: Perfect):179,653,236-179,658,535Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6645730Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1179,684,101179,689,400
    nsv6645730RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1179,653,236179,658,535

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18571891duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18571891Submitted genomicNC_000001.11:g.179
    684101_179689400du
    p
    GRCh38 (hg38)NC_000001.11Chr1179,684,101179,689,400
    nssv18571891RemappedPerfectNC_000001.10:g.179
    653236_179658535du
    p
    GRCh37.p13First PassNC_000001.10Chr1179,653,236179,658,535

    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)
    nssv185718910.003951265976
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