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nsv6316348

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:72,885

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 285 SVs from 43 studies. See in: genome view    
    Submitted genomic205,368,397-205,441,281Question Mark
    Overlapping variant regions from other studies: 285 SVs from 43 studies. See in: genome view    
    Remapped(Score: Perfect):205,337,525-205,410,409Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6316348Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1205,368,397205,441,281
    nsv6316348RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1205,337,525205,410,409

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18201864duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18201864Submitted genomicNC_000001.11:g.205
    368397_205441281du
    p
    GRCh38 (hg38)NC_000001.11Chr1205,368,397205,441,281
    nssv18201864RemappedPerfectNC_000001.10:g.205
    337525_205410409du
    p
    GRCh37.p13First PassNC_000001.10Chr1205,337,525205,410,409

    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)
    nssv18201864<0.001139304
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