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nsv6850328

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:18,471

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 208 SVs from 35 studies. See in: genome view    
    Submitted genomic30,362,776-30,381,246Question Mark
    Overlapping variant regions from other studies: 208 SVs from 35 studies. See in: genome view    
    Remapped(Score: Perfect):30,220,292-30,238,762Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6850328Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr830,362,77630,381,246
    nsv6850328RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr830,220,29230,238,762

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18555269deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18555269Submitted genomicNC_000008.11:g.303
    62776_30381246del
    GRCh38 (hg38)NC_000008.11Chr830,362,77630,381,246
    nssv18555269RemappedPerfectNC_000008.10:g.302
    20292_30238762del
    GRCh37.p13First PassNC_000008.10Chr830,220,29230,238,762

    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)
    nssv185552694e-061276136
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