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nsv6845044

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:10,639

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 179 SVs from 28 studies. See in: genome view    
    Submitted genomic30,589,065-30,599,703Question Mark
    Overlapping variant regions from other studies: 179 SVs from 28 studies. See in: genome view    
    Remapped(Score: Perfect):30,446,582-30,457,220Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6845044Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr830,589,06530,599,703
    nsv6845044RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr830,446,58230,457,220

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18555294deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18555294Submitted genomicNC_000008.11:g.305
    89065_30599703del
    GRCh38 (hg38)NC_000008.11Chr830,589,06530,599,703
    nssv18555294RemappedPerfectNC_000008.10:g.304
    46582_30457220del
    GRCh37.p13First PassNC_000008.10Chr830,446,58230,457,220

    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)
    nssv185552944e-061276266
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