A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3584756



Internal ID18536351
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:36855609..36916270hg38UCSC Ensembl
Innerchr20:35484012..35544673hg19UCSC Ensembl
Innerchr20:34917426..34978087hg18UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg3860662
hg1960662
hg1860662
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1057845
Supporting Variants
Samples
Known GenesSAMHD1, SOGA1, TLDC2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3584756
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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