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nsv6735504

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:61

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 138 SVs from 26 studies. See in: genome view    
    Submitted genomic195,209,961-195,210,021Question Mark
    Overlapping variant regions from other studies: 138 SVs from 26 studies. See in: genome view    
    Remapped(Score: Perfect):194,930,690-194,930,750Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6735504Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3195,209,961195,210,021
    nsv6735504RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3194,930,690194,930,750

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18677353duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18677353Submitted genomicNC_000003.12:g.195
    209961_195210021du
    p
    GRCh38 (hg38)NC_000003.12Chr3195,209,961195,210,021
    nssv18677353RemappedPerfectNC_000003.11:g.194
    930690_194930750du
    p
    GRCh37.p13First PassNC_000003.11Chr3194,930,690194,930,750

    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)
    nssv186773530.0142777210752
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