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nsv6385163

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:487

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 115 SVs from 21 studies. See in: genome view    
    Submitted genomic129,739,881-129,740,367Question Mark
    Overlapping variant regions from other studies: 115 SVs from 21 studies. See in: genome view    
    Remapped(Score: Perfect):130,661,036-130,661,522Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6385163Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr4129,739,881129,740,367
    nsv6385163RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr4130,661,036130,661,522

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18111195deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18111195Submitted genomicNC_000004.12:g.129
    739881_129740367de
    l
    GRCh38 (hg38)NC_000004.12Chr4129,739,881129,740,367
    nssv18111195RemappedPerfectNC_000004.11:g.130
    661036_130661522de
    l
    GRCh37.p13First PassNC_000004.11Chr4130,661,036130,661,522

    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)
    nssv18111195<0.0012537066
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