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nsv6792696

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,400

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 228 SVs from 46 studies. See in: genome view    
    Submitted genomic34,350,401-34,351,800Question Mark
    Overlapping variant regions from other studies: 228 SVs from 46 studies. See in: genome view    
    Remapped(Score: Perfect):34,318,178-34,319,577Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6792696Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr634,350,40134,351,800
    nsv6792696RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr634,318,17834,319,577

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18527259deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18527259Submitted genomicNC_000006.12:g.343
    50401_34351800del
    GRCh38 (hg38)NC_000006.12Chr634,350,40134,351,800
    nssv18527259RemappedPerfectNC_000006.11:g.343
    18178_34319577del
    GRCh37.p13First PassNC_000006.11Chr634,318,17834,319,577

    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)
    nssv185272590.001285236786
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