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nsv6781511

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,449,660

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 8202 SVs from 99 studies. See in: genome view    
    Submitted genomic170,662,244-174,111,903Question Mark
    Overlapping variant regions from other studies: 8202 SVs from 99 studies. See in: genome view    
    Remapped(Score: Perfect):170,089,248-173,538,906Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6781511Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5170,662,244174,111,903
    nsv6781511RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5170,089,248173,538,906

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18510561deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18510561Submitted genomicNC_000005.10:g.170
    662244_174111903de
    l
    GRCh38 (hg38)NC_000005.10Chr5170,662,244174,111,903
    nssv18510561RemappedPerfectNC_000005.9:g.1700
    89248_173538906del
    GRCh37.p13First PassNC_000005.9Chr5170,089,248173,538,906

    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)
    nssv185105614e-061275406
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