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nsv6439797

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,219

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 98 SVs from 23 studies. See in: genome view    
    Submitted genomic86,127,871-86,130,089Question Mark
    Overlapping variant regions from other studies: 98 SVs from 23 studies. See in: genome view    
    Remapped(Score: Perfect):88,742,786-88,745,004Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6439797Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr986,127,87186,130,089
    nsv6439797RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr988,742,78688,745,004

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18184475deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18184475Submitted genomicNC_000009.12:g.861
    27871_86130089del
    GRCh38 (hg38)NC_000009.12Chr986,127,87186,130,089
    nssv18184475RemappedPerfectNC_000009.11:g.887
    42786_88745004del
    GRCh37.p13First PassNC_000009.11Chr988,742,78688,745,004

    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)
    nssv18184475<0.001938622
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