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nsv7044054

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:348,624

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 948 SVs from 64 studies. See in: genome view    
    Submitted genomic152,619,891-152,968,514Question Mark
    Overlapping variant regions from other studies: 948 SVs from 64 studies. See in: genome view    
    Remapped(Score: Perfect):153,541,043-153,889,666Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7044054Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr4152,619,891152,968,514
    nsv7044054RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr4153,541,043153,889,666

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18772733inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18772733Submitted genomicNC_000004.12:g.152
    619891_152968514in
    v
    GRCh38 (hg38)NC_000004.12Chr4152,619,891152,968,514
    nssv18772733RemappedPerfectNC_000004.11:g.153
    541043_153889666in
    v
    GRCh37.p13First PassNC_000004.11Chr4153,541,043153,889,666

    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)
    nssv187727334e-061276268
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