U.S. flag

An official website of the United States government

nsv7067217

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:93,474

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 496 SVs from 58 studies. See in: genome view    
    Submitted genomic19,708,681-19,802,154Question Mark
    Overlapping variant regions from other studies: 496 SVs from 58 studies. See in: genome view    
    Remapped(Score: Perfect):19,611,994-19,705,467Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7067217Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1719,708,68119,802,154
    nsv7067217RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1719,611,99419,705,467

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18756230inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18756230Submitted genomicNC_000017.11:g.197
    08681_19802154inv
    GRCh38 (hg38)NC_000017.11Chr1719,708,68119,802,154
    nssv18756230RemappedPerfectNC_000017.10:g.196
    11994_19705467inv
    GRCh37.p13First PassNC_000017.10Chr1719,611,99419,705,467

    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)
    nssv187562307e-062274740
    Support Center