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nsv6328538

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:138,862

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 450 SVs from 50 studies. See in: genome view    
    Submitted genomic153,953,287-154,092,148Question Mark
    Overlapping variant regions from other studies: 461 SVs from 51 studies. See in: genome view    
    Remapped(Score: Perfect):153,925,763-154,064,624Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6328538Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1153,953,287154,092,148
    nsv6328538RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1153,925,763154,064,624

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18200495duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18200495Submitted genomicNC_000001.11:g.153
    953287_154092148du
    p
    GRCh38 (hg38)NC_000001.11Chr1153,953,287154,092,148
    nssv18200495RemappedPerfectNC_000001.10:g.153
    925763_154064624du
    p
    GRCh37.p13First PassNC_000001.10Chr1153,925,763154,064,624

    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)
    nssv18200495<0.001139302
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