A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026091



Internal ID18768623
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:18441326..18617605hg38UCSC Ensembl
Innerchr8:18298836..18475115hg19UCSC Ensembl
Innerchr8:18343116..18519395hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg38176280
hg19176280
hg18176280
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3684194
Samples
Known GenesPSD3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1026091
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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