U.S. flag

An official website of the United States government

nsv6750028

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:6,166

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 178 SVs from 35 studies. See in: genome view    
    Submitted genomic164,792,917-164,799,082Question Mark
    Overlapping variant regions from other studies: 178 SVs from 35 studies. See in: genome view    
    Remapped(Score: Perfect):165,714,069-165,720,234Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6750028Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr4164,792,917164,799,082
    nsv6750028RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr4165,714,069165,720,234

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18494184deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18494184Submitted genomicNC_000004.12:g.164
    792917_164799082de
    l
    GRCh38 (hg38)NC_000004.12Chr4164,792,917164,799,082
    nssv18494184RemappedPerfectNC_000004.11:g.165
    714069_165720234de
    l
    GRCh37.p13First PassNC_000004.11Chr4165,714,069165,720,234

    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)
    nssv184941844e-061276110
    Support Center