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nsv6997761

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,114

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 310 SVs from 58 studies. See in: genome view    
    Submitted genomic22,357,158-22,359,271Question Mark
    Overlapping variant regions from other studies: 310 SVs from 58 studies. See in: genome view    
    Remapped(Score: Perfect):22,368,479-22,370,592Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6997761Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr1622,357,15822,359,271
    nsv6997761RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr1622,368,47922,370,592

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18620129duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18620129Submitted genomicNC_000016.10:g.223
    57158_22359271dup
    GRCh38 (hg38)NC_000016.10Chr1622,357,15822,359,271
    nssv18620129RemappedPerfectNC_000016.9:g.2236
    8479_22370592dup
    GRCh37.p13First PassNC_000016.9Chr1622,368,47922,370,592

    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)
    nssv18620129<0.001121267268
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