A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3566457



Internal ID18864738
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:68032457..68298509hg38UCSC Ensembl
Innerchr18:65699694..65965746hg19UCSC Ensembl
Innerchr18:63850674..64116726hg18UCSC Ensembl
Cytoband18q22.1
Allele length
AssemblyAllele length
hg38266053
hg19266053
hg18266053
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1064445
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3566457
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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