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nsv6396672

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,300

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 207 SVs from 53 studies. See in: genome view    
    Submitted genomic31,266,301-31,267,600Question Mark
    Overlapping variant regions from other studies: 207 SVs from 53 studies. See in: genome view    
    Remapped(Score: Perfect):31,234,078-31,235,377Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6396672Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr631,266,30131,267,600
    nsv6396672RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr631,234,07831,235,377

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18142073deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18142073Submitted genomicNC_000006.12:g.312
    66301_31267600del
    GRCh38 (hg38)NC_000006.12Chr631,266,30131,267,600
    nssv18142073RemappedPerfectNC_000006.11:g.312
    34078_31235377del
    GRCh37.p13First PassNC_000006.11Chr631,234,07831,235,377

    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)
    nssv18142073<0.001137524
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