U.S. flag

An official website of the United States government

nsv6726452

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:28,200

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 142 SVs from 40 studies. See in: genome view    
    Submitted genomic44,021,901-44,050,100Question Mark
    Overlapping variant regions from other studies: 142 SVs from 40 studies. See in: genome view    
    Remapped(Score: Perfect):44,023,918-44,052,117Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6726452Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr444,021,90144,050,100
    nsv6726452RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr444,023,91844,052,117

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18495397deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18495397Submitted genomicNC_000004.12:g.440
    21901_44050100del
    GRCh38 (hg38)NC_000004.12Chr444,021,90144,050,100
    nssv18495397RemappedPerfectNC_000004.11:g.440
    23918_44052117del
    GRCh37.p13First PassNC_000004.11Chr444,023,91844,052,117

    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)
    nssv18495397<0.001120245256
    Support Center