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nsv6814349

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:586

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 177 SVs from 36 studies. See in: genome view    
    Submitted genomic2,691,128-2,691,713Question Mark
    Overlapping variant regions from other studies: 177 SVs from 36 studies. See in: genome view    
    Remapped(Score: Perfect):2,730,762-2,731,347Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6814349Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr72,691,1282,691,713
    nsv6814349RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr72,730,7622,731,347

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18543517deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18543517Submitted genomicNC_000007.14:g.269
    1128_2691713del
    GRCh38 (hg38)NC_000007.14Chr72,691,1282,691,713
    nssv18543517RemappedPerfectNC_000007.13:g.273
    0762_2731347del
    GRCh37.p13First PassNC_000007.13Chr72,730,7622,731,347

    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)
    nssv185435170.0716690248302
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