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nsv6452172

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:360,474

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 746 SVs from 69 studies. See in: genome view    
    Submitted genomic123,089,191-123,449,664Question Mark
    Overlapping variant regions from other studies: 746 SVs from 69 studies. See in: genome view    
    Remapped(Score: Perfect):124,848,707-125,209,180Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6452172Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr10123,089,191123,449,664
    nsv6452172RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr10124,848,707125,209,180

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18195043duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18195043Submitted genomicNC_000010.11:g.123
    089191_123449664du
    p
    GRCh38 (hg38)NC_000010.11Chr10123,089,191123,449,664
    nssv18195043RemappedPerfectNC_000010.10:g.124
    848707_125209180du
    p
    GRCh37.p13First PassNC_000010.10Chr10124,848,707125,209,180

    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)
    nssv18195043<0.001139304
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