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nsv4157202

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:193,340

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 254 SVs from 16 studies. See in: genome view    
Remapped(Score: Perfect):17,568,744-17,762,083Question Mark
Overlapping variant regions from other studies: 254 SVs from 16 studies. See in: genome view    
Submitted genomic17,426,253-17,619,592Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4157202RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000008.11Chr817,568,74417,762,083
nsv4157202Submitted genomicGRCh37.p13Primary AssemblyNC_000008.10Chr817,426,25317,619,592

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv15983488duplicationSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv15983488RemappedPerfectNC_000008.11:g.175
68744_17762083dup
GRCh38.p12First PassNC_000008.11Chr817,568,74417,762,083
nssv15983488Submitted genomicNC_000008.10:g.174
26253_17619592dup
GRCh37.p13NC_000008.10Chr817,426,25317,619,592

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)
nssv159834884.6e-005121694
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