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nsv7045756

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:242

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 271 SVs from 26 studies. See in: genome view    
    Submitted genomic185,161,194-185,161,435Question Mark
    Overlapping variant regions from other studies: 271 SVs from 26 studies. See in: genome view    
    Remapped(Score: Perfect):186,082,348-186,082,589Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7045756Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr4185,161,194185,161,435
    nsv7045756RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr4186,082,348186,082,589

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18774014inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18774014Submitted genomicNC_000004.12:g.185
    161194_185161435in
    v
    GRCh38 (hg38)NC_000004.12Chr4185,161,194185,161,435
    nssv18774014RemappedPerfectNC_000004.11:g.186
    082348_186082589in
    v
    GRCh37.p13First PassNC_000004.11Chr4186,082,348186,082,589

    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)
    nssv18774014<0.00140274516
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