U.S. flag

An official website of the United States government

nsv6449826

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:47,500

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 208 SVs from 41 studies. See in: genome view    
    Submitted genomic22,312,201-22,359,700Question Mark
    Overlapping variant regions from other studies: 208 SVs from 41 studies. See in: genome view    
    Remapped(Score: Perfect):22,601,130-22,648,629Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6449826Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr1022,312,20122,359,700
    nsv6449826RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr1022,601,13022,648,629

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18183584duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18183584Submitted genomicNC_000010.11:g.223
    12201_22359700dup
    GRCh38 (hg38)NC_000010.11Chr1022,312,20122,359,700
    nssv18183584RemappedPerfectNC_000010.10:g.226
    01130_22648629dup
    GRCh37.p13First PassNC_000010.10Chr1022,601,13022,648,629

    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)
    nssv18183584<0.0012539248
    Support Center