A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3584663



Internal ID18536258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:23432253..23588601hg38UCSC Ensembl
Innerchr20:23412890..23569238hg19UCSC Ensembl
Innerchr20:23360890..23517238hg18UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg38156349
hg19156349
hg18156349
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1065390
Supporting Variants
Samples
Known GenesCST11, CST13P, CST8, CST9L, CSTL1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3584663
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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