A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3584679



Internal ID18536274
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:25086650..25494993hg38UCSC Ensembl
Innerchr20:25067286..25475629hg19UCSC Ensembl
Innerchr20:25015286..25423629hg18UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg38408344
hg19408344
hg18408344
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1063016
Supporting Variants
Samples
Known GenesABHD12, ENTPD6, GINS1, LOC284798, NINL, PYGB
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3584679
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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