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nsv6794984

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,985,823

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 9362 SVs from 103 studies. See in: genome view    
    Submitted genomic159,275,371-163,261,193Question Mark
    Overlapping variant regions from other studies: 9362 SVs from 103 studies. See in: genome view    
    Remapped(Score: Perfect):158,702,379-162,688,199Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6794984Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5159,275,371163,261,193
    nsv6794984RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5158,702,379162,688,199

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18509847deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18509847Submitted genomicNC_000005.10:g.159
    275371_163261193de
    l
    GRCh38 (hg38)NC_000005.10Chr5159,275,371163,261,193
    nssv18509847RemappedPerfectNC_000005.9:g.1587
    02379_162688199del
    GRCh37.p13First PassNC_000005.9Chr5158,702,379162,688,199

    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)
    nssv185098474e-061275810
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