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nsv6397911

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:294

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 87 SVs from 18 studies. See in: genome view    
    Submitted genomic146,212,084-146,212,377Question Mark
    Overlapping variant regions from other studies: 87 SVs from 18 studies. See in: genome view    
    Remapped(Score: Perfect):145,591,647-145,591,940Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6397911Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5146,212,084146,212,377
    nsv6397911RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5145,591,647145,591,940

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18126039deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18126039Submitted genomicNC_000005.10:g.146
    212084_146212377de
    l
    GRCh38 (hg38)NC_000005.10Chr5146,212,084146,212,377
    nssv18126039RemappedPerfectNC_000005.9:g.1455
    91647_145591940del
    GRCh37.p13First PassNC_000005.9Chr5145,591,647145,591,940

    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)
    nssv18126039<0.001132110
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