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nsv6736253

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:265

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 220 SVs from 32 studies. See in: genome view    
    Submitted genomic4,205,330-4,205,594Question Mark
    Overlapping variant regions from other studies: 220 SVs from 32 studies. See in: genome view    
    Remapped(Score: Perfect):4,207,057-4,207,321Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6736253Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr44,205,3304,205,594
    nsv6736253RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr44,207,0574,207,321

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18690125duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18690125Submitted genomicNC_000004.12:g.420
    5330_4205594dup
    GRCh38 (hg38)NC_000004.12Chr44,205,3304,205,594
    nssv18690125RemappedPerfectNC_000004.11:g.420
    7057_4207321dup
    GRCh37.p13First PassNC_000004.11Chr44,207,0574,207,321

    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)
    nssv186901252.4e-056242944
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