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nsv6644404

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,238

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 203 SVs from 50 studies. See in: genome view    
    Submitted genomic169,553,825-169,559,062Question Mark
    Overlapping variant regions from other studies: 206 SVs from 50 studies. See in: genome view    
    Remapped(Score: Perfect):169,523,063-169,528,300Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6644404Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1169,553,825169,559,062
    nsv6644404RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1169,523,063169,528,300

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18363264deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18363264Submitted genomicNC_000001.11:g.169
    553825_169559062de
    l
    GRCh38 (hg38)NC_000001.11Chr1169,553,825169,559,062
    nssv18363264RemappedPerfectNC_000001.10:g.169
    523063_169528300de
    l
    GRCh37.p13First PassNC_000001.10Chr1169,523,063169,528,300

    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)
    nssv183632647e-062276118
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