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nsv6352542

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,678

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 120 SVs from 28 studies. See in: genome view    
    Submitted genomic101,403,635-101,408,312Question Mark
    Overlapping variant regions from other studies: 120 SVs from 28 studies. See in: genome view    
    Remapped(Score: Perfect):102,020,097-102,024,774Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6352542Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2101,403,635101,408,312
    nsv6352542RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2102,020,097102,024,774

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18205770duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18205770Submitted genomicNC_000002.12:g.101
    403635_101408312du
    p
    GRCh38 (hg38)NC_000002.12Chr2101,403,635101,408,312
    nssv18205770RemappedPerfectNC_000002.11:g.102
    020097_102024774du
    p
    GRCh37.p13First PassNC_000002.11Chr2102,020,097102,024,774

    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)
    nssv18205770<0.001439278
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