nsv6805752

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,100

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 118 SVs from 24 studies. See in: genome view    
    Submitted genomic110,433,801-110,437,900Question Mark
    Overlapping variant regions from other studies: 118 SVs from 24 studies. See in: genome view    
    Remapped(Score: Perfect):110,755,004-110,759,103Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6805752Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr6110,433,801110,437,900
    nsv6805752RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr6110,755,004110,759,103

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18521718deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18521718Submitted genomicNC_000006.12:g.110
    433801_110437900de
    l
    GRCh38 (hg38)NC_000006.12Chr6110,433,801110,437,900
    nssv18521718RemappedPerfectNC_000006.11:g.110
    755004_110759103de
    l
    GRCh37.p13First PassNC_000006.11Chr6110,755,004110,759,103

    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)
    nssv185217184e-061275990
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