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nsv7034017

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:6,466

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 191 SVs from 35 studies. See in: genome view    
    Submitted genomic39,589,985-39,596,450Question Mark
    Overlapping variant regions from other studies: 192 SVs from 35 studies. See in: genome view    
    Remapped(Score: Perfect):40,961,912-40,968,377Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7034017Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000021.9Chr2139,589,98539,596,450
    nsv7034017RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000021.8Chr2140,961,91240,968,377

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18436378deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18436378Submitted genomicNC_000021.9:g.3958
    9985_39596450del
    GRCh38 (hg38)NC_000021.9Chr2139,589,98539,596,450
    nssv18436378RemappedPerfectNC_000021.8:g.4096
    1912_40968377del
    GRCh37.p13First PassNC_000021.8Chr2140,961,91240,968,377

    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)
    nssv184363784e-061276250
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