A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3589962



Internal ID18888243
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:706472..739210hg38UCSC Ensembl
Innerchr20:687116..719854hg19UCSC Ensembl
Innerchr20:635116..667854hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3832739
hg1932739
hg1832739
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1060201
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)nssv3589962
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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