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nsv6827172

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,616

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 181 SVs from 32 studies. See in: genome view    
    Submitted genomic149,719,901-149,724,516Question Mark
    Overlapping variant regions from other studies: 181 SVs from 32 studies. See in: genome view    
    Remapped(Score: Perfect):149,416,992-149,421,607Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6827172Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr7149,719,901149,724,516
    nsv6827172RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr7149,416,992149,421,607

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18537312deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18537312Submitted genomicNC_000007.14:g.149
    719901_149724516de
    l
    GRCh38 (hg38)NC_000007.14Chr7149,719,901149,724,516
    nssv18537312RemappedPerfectNC_000007.13:g.149
    416992_149421607de
    l
    GRCh37.p13First PassNC_000007.13Chr7149,416,992149,421,607

    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)
    nssv185373121.1e-053276246
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