U.S. flag

An official website of the United States government

nsv7062507

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,904

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 108 SVs from 33 studies. See in: genome view    
    Submitted genomic96,212,860-96,217,763Question Mark
    Overlapping variant regions from other studies: 108 SVs from 33 studies. See in: genome view    
    Remapped(Score: Perfect):96,679,197-96,684,100Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7062507Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000014.9Chr1496,212,86096,217,763
    nsv7062507RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000014.8Chr1496,679,19796,684,100

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18755389inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18755389Submitted genomicNC_000014.9:g.9621
    2860_96217763inv
    GRCh38 (hg38)NC_000014.9Chr1496,212,86096,217,763
    nssv18755389RemappedPerfectNC_000014.8:g.9667
    9197_96684100inv
    GRCh37.p13First PassNC_000014.8Chr1496,679,19796,684,100

    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)
    nssv187553890.004953274688
    Support Center