U.S. flag

An official website of the United States government

nsv6706135

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,113

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 73 SVs from 17 studies. See in: genome view    
    Submitted genomic15,594,394-15,595,506Question Mark
    Overlapping variant regions from other studies: 73 SVs from 17 studies. See in: genome view    
    Remapped(Score: Perfect):15,635,901-15,637,013Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6706135Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr315,594,39415,595,506
    nsv6706135RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr315,635,90115,637,013

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18475323deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18475323Submitted genomicNC_000003.12:g.155
    94394_15595506del
    GRCh38 (hg38)NC_000003.12Chr315,594,39415,595,506
    nssv18475323RemappedPerfectNC_000003.11:g.156
    35901_15637013del
    GRCh37.p13First PassNC_000003.11Chr315,635,90115,637,013

    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)
    nssv184753233.9e-0510252270
    Support Center