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nsv6439915

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:39,556

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 237 SVs from 47 studies. See in: genome view    
    Submitted genomic104,050,471-104,090,026Question Mark
    Overlapping variant regions from other studies: 237 SVs from 47 studies. See in: genome view    
    Remapped(Score: Perfect):106,812,752-106,852,307Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6439915Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr9104,050,471104,090,026
    nsv6439915RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr9106,812,752106,852,307

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18172624deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18172624Submitted genomicNC_000009.12:g.104
    050471_104090026de
    l
    GRCh38 (hg38)NC_000009.12Chr9104,050,471104,090,026
    nssv18172624RemappedPerfectNC_000009.11:g.106
    812752_106852307de
    l
    GRCh37.p13First PassNC_000009.11Chr9106,812,752106,852,307

    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)
    nssv18172624<0.0012139212
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