U.S. flag

An official website of the United States government

nsv6643147

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,296

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 135 SVs from 26 studies. See in: genome view    
    Submitted genomic160,993,643-160,996,938Question Mark
    Overlapping variant regions from other studies: 139 SVs from 26 studies. See in: genome view    
    Remapped(Score: Perfect):160,963,433-160,966,728Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6643147Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1160,993,643160,996,938
    nsv6643147RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1160,963,433160,966,728

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18363463deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18363463Submitted genomicNC_000001.11:g.160
    993643_160996938de
    l
    GRCh38 (hg38)NC_000001.11Chr1160,993,643160,996,938
    nssv18363463RemappedPerfectNC_000001.10:g.160
    963433_160966728de
    l
    GRCh37.p13First PassNC_000001.10Chr1160,963,433160,966,728

    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)
    nssv183634631.1e-053275768
    Support Center