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nsv6935164

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:53

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 128 SVs from 25 studies. See in: genome view    
    Submitted genomic14,577,122-14,577,174Question Mark
    Overlapping variant regions from other studies: 129 SVs from 25 studies. See in: genome view    
    Remapped(Score: Perfect):14,730,056-14,730,108Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6935164Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1214,577,12214,577,174
    nsv6935164RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1214,730,05614,730,108

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18358319deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18358319Submitted genomicNC_000012.12:g.145
    77122_14577174del
    GRCh38 (hg38)NC_000012.12Chr1214,577,12214,577,174
    nssv18358319RemappedPerfectNC_000012.11:g.147
    30056_14730108del
    GRCh37.p13First PassNC_000012.11Chr1214,730,05614,730,108

    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)
    nssv18358319<0.00161238734
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