U.S. flag

An official website of the United States government

nsv6751314

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:125,700

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1027 SVs from 85 studies. See in: genome view    
    Submitted genomic143,898,601-144,024,300Question Mark
    Overlapping variant regions from other studies: 1027 SVs from 85 studies. See in: genome view    
    Remapped(Score: Perfect):144,819,754-144,945,453Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6751314Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr4143,898,601144,024,300
    nsv6751314RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr4144,819,754144,945,453

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18488696deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18488696Submitted genomicNC_000004.12:g.143
    898601_144024300de
    l
    GRCh38 (hg38)NC_000004.12Chr4143,898,601144,024,300
    nssv18488696RemappedPerfectNC_000004.11:g.144
    819754_144945453de
    l
    GRCh37.p13First PassNC_000004.11Chr4144,819,754144,945,453

    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)
    nssv184886960.0174128260206
    Support Center