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nsv6894711

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:8,500

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 395 SVs from 40 studies. See in: genome view    
    Submitted genomic136,548,601-136,557,100Question Mark
    Overlapping variant regions from other studies: 395 SVs from 40 studies. See in: genome view    
    Remapped(Score: Perfect):139,443,053-139,451,552Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6894711Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr9136,548,601136,557,100
    nsv6894711RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr9139,443,053139,451,552

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18563723deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18563723Submitted genomicNC_000009.12:g.136
    548601_136557100de
    l
    GRCh38 (hg38)NC_000009.12Chr9136,548,601136,557,100
    nssv18563723RemappedPerfectNC_000009.11:g.139
    443053_139451552de
    l
    GRCh37.p13First PassNC_000009.11Chr9139,443,053139,451,552

    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)
    nssv18563723<0.001132253010
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