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nsv4314197

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,073,560

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 719 SVs from 19 studies. See in: genome view    
Remapped(Score: Perfect):86,353,829-87,427,388Question Mark
Overlapping variant regions from other studies: 719 SVs from 19 studies. See in: genome view    
Submitted genomic88,968,744-90,042,303Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4314197RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000009.12Chr986,353,82987,427,388
nsv4314197Submitted genomicGRCh37.p13Primary AssemblyNC_000009.11Chr988,968,74490,042,303

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16090453inversionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16090453RemappedPerfectNC_000009.12:g.863
53829_87427388inv
GRCh38.p12First PassNC_000009.12Chr986,353,82987,427,388
nssv16090453Submitted genomicNC_000009.11:g.889
68744_90042303inv
GRCh37.p13NC_000009.11Chr988,968,74490,042,303

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)
nssv160904534.6e-005121694
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