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nsv7072391

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:7,516

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 154 SVs from 24 studies. See in: genome view    
    Submitted genomic37,597,154-37,604,669Question Mark
    Overlapping variant regions from other studies: 161 SVs from 25 studies. See in: genome view    
    Remapped(Score: Perfect):37,597,151-37,604,666Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7072391Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr937,597,15437,604,669
    nsv7072391RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr937,597,15137,604,666

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18783951inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18783951Submitted genomicNC_000009.12:g.375
    97154_37604669inv
    GRCh38 (hg38)NC_000009.12Chr937,597,15437,604,669
    nssv18783951RemappedPerfectNC_000009.11:g.375
    97151_37604666inv
    GRCh37.p13First PassNC_000009.11Chr937,597,15137,604,666

    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)
    nssv187839514e-061276266
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