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nsv7045450

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,271

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 169 SVs from 34 studies. See in: genome view    
    Submitted genomic76,519,770-76,525,040Question Mark
    Overlapping variant regions from other studies: 169 SVs from 34 studies. See in: genome view    
    Remapped(Score: Perfect):76,985,455-76,990,725Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7045450Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr176,519,77076,525,040
    nsv7045450RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr176,985,45576,990,725

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18762477inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18762477Submitted genomicNC_000001.11:g.765
    19770_76525040inv
    GRCh38 (hg38)NC_000001.11Chr176,519,77076,525,040
    nssv18762477RemappedPerfectNC_000001.10:g.769
    85455_76990725inv
    GRCh37.p13First PassNC_000001.10Chr176,985,45576,990,725

    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)
    nssv187624775.3e-0514274784
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