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nsv6750623

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:481,391

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 2091 SVs from 92 studies. See in: genome view    
    Submitted genomic164,776,894-165,258,284Question Mark
    Overlapping variant regions from other studies: 2091 SVs from 92 studies. See in: genome view    
    Remapped(Score: Perfect):165,698,046-166,179,436Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6750623Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr4164,776,894165,258,284
    nsv6750623RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr4165,698,046166,179,436

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18685613duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18685613Submitted genomicNC_000004.12:g.164
    776894_165258284du
    p
    GRCh38 (hg38)NC_000004.12Chr4164,776,894165,258,284
    nssv18685613RemappedPerfectNC_000004.11:g.165
    698046_166179436du
    p
    GRCh37.p13First PassNC_000004.11Chr4165,698,046166,179,436

    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)
    nssv186856134e-061265566
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