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nsv6756183

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:107,200

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 480 SVs from 59 studies. See in: genome view    
    Submitted genomic83,478,901-83,586,100Question Mark
    Overlapping variant regions from other studies: 480 SVs from 59 studies. See in: genome view    
    Remapped(Score: Perfect):84,400,054-84,507,253Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6756183Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr483,478,90183,586,100
    nsv6756183RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr484,400,05484,507,253

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18694380duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18694380Submitted genomicNC_000004.12:g.834
    78901_83586100dup
    GRCh38 (hg38)NC_000004.12Chr483,478,90183,586,100
    nssv18694380RemappedPerfectNC_000004.11:g.844
    00054_84507253dup
    GRCh37.p13First PassNC_000004.11Chr484,400,05484,507,253

    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)
    nssv186943804e-061274690
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