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nsv6444927

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:13,608

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 127 SVs from 26 studies. See in: genome view    
    Submitted genomic69,264,305-69,277,912Question Mark
    Overlapping variant regions from other studies: 127 SVs from 26 studies. See in: genome view    
    Remapped(Score: Perfect):71,024,061-71,037,668Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6444927Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr1069,264,30569,277,912
    nsv6444927RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr1071,024,06171,037,668

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18195295duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18195295Submitted genomicNC_000010.11:g.692
    64305_69277912dup
    GRCh38 (hg38)NC_000010.11Chr1069,264,30569,277,912
    nssv18195295RemappedPerfectNC_000010.10:g.710
    24061_71037668dup
    GRCh37.p13First PassNC_000010.10Chr1071,024,06171,037,668

    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)
    nssv18195295<0.001139268
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