A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3584762



Internal ID18536357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:37386619..37461537hg38UCSC Ensembl
Innerchr20:36015022..36089939hg19UCSC Ensembl
Innerchr20:35448436..35523353hg18UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg3874919
hg1974918
hg1874918
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1060900
Supporting Variants
Samples
Known GenesSRC
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3584762
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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