A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv981214



Internal ID16275170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:170057033..170215221hg38UCSC Ensembl
Innerchr3:169774821..169933009hg19UCSC Ensembl
Innerchr3:171257515..171415703hg18UCSC Ensembl
Cytoband3q26.2
Allele length
AssemblyAllele length
hg38158189
hg19158189
hg18158189
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv592507
Supporting Variants
Samples
Known GenesGPR160, PHC3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv981214
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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