U.S. flag

An official website of the United States government

nsv7074771

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:31

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 151 SVs from 12 studies. See in: genome view    
    Submitted genomic102,369,706-102,369,736Question Mark
    Overlapping variant regions from other studies: 151 SVs from 12 studies. See in: genome view    
    Remapped(Score: Perfect):103,022,056-103,022,086Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7074771Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000013.11Chr13102,369,706102,369,736
    nsv7074771RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000013.10Chr13103,022,056103,022,086

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18752010inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18752010Submitted genomicNC_000013.11:g.102
    369706_102369736in
    v
    GRCh38 (hg38)NC_000013.11Chr13102,369,706102,369,736
    nssv18752010RemappedPerfectNC_000013.10:g.103
    022056_103022086in
    v
    GRCh37.p13First PassNC_000013.10Chr13103,022,056103,022,086

    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)
    nssv18752010<0.00154274056
    Support Center