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nsv6672160

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,001

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 144 SVs from 29 studies. See in: genome view    
    Submitted genomic233,336,831-233,341,831Question Mark
    Overlapping variant regions from other studies: 147 SVs from 29 studies. See in: genome view    
    Remapped(Score: Perfect):233,472,577-233,477,577Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6672160Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1233,336,831233,341,831
    nsv6672160RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1233,472,577233,477,577

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18370263deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18370263Submitted genomicNC_000001.11:g.233
    336831_233341831de
    l
    GRCh38 (hg38)NC_000001.11Chr1233,336,831233,341,831
    nssv18370263RemappedPerfectNC_000001.10:g.233
    472577_233477577de
    l
    GRCh37.p13First PassNC_000001.10Chr1233,472,577233,477,577

    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)
    nssv183702634e-061276074
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