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nsv6373585

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:443

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 73 SVs from 15 studies. See in: genome view    
    Submitted genomic44,425,793-44,426,235Question Mark
    Overlapping variant regions from other studies: 73 SVs from 15 studies. See in: genome view    
    Remapped(Score: Perfect):44,467,285-44,467,727Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6373585Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr344,425,79344,426,235
    nsv6373585RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr344,467,28544,467,727

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18209265duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18209265Submitted genomicNC_000003.12:g.444
    25793_44426235dup
    GRCh38 (hg38)NC_000003.12Chr344,425,79344,426,235
    nssv18209265RemappedPerfectNC_000003.11:g.444
    67285_44467727dup
    GRCh37.p13First PassNC_000003.11Chr344,467,28544,467,727

    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)
    nssv18209265<0.001138136
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