A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3599640



Internal ID18897921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:16201211..16215152hg38UCSC Ensembl
Innerchr20:16181856..16195797hg19UCSC Ensembl
Innerchr20:16129856..16143797hg18UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg3813942
hg1913942
hg1813942
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1057504
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)nssv3599640
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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