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nsv7063700

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:7,106,960

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 17729 SVs from 113 studies. See in: genome view    
    Submitted genomic48,591,726-55,698,685Question Mark
    Overlapping variant regions from other studies: 17709 SVs from 113 studies. See in: genome view    
    Remapped(Score: Good):49,060,929-56,165,403Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7063700Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000014.9Chr1448,591,72655,698,685
    nsv7063700RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000014.8Chr1449,060,92956,165,403

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18756255inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18756255Submitted genomicNC_000014.9:g.4859
    1726_55698685inv
    GRCh38 (hg38)NC_000014.9Chr1448,591,72655,698,685
    nssv18756255RemappedGoodNC_000014.8:g.4906
    0929_56165403inv
    GRCh37.p13First PassNC_000014.8Chr1449,060,92956,165,403

    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)
    nssv187562554e-061276268
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