A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1107413



Internal ID15613913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:18564808..18580219hg38UCSC Ensembl
Innerchr8:18422318..18437729hg19UCSC Ensembl
Innerchr8:18466598..18482009hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3815412
hg1915412
hg1815412
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv610718
Supporting Variants
Samples
Known GenesPSD3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1107413
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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