A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3521920



Internal ID18820201
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:7821395..7978362hg38UCSC Ensembl
Innerchr12:7973991..8130958hg19UCSC Ensembl
Innerchr12:7865258..8022225hg18UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg38156968
hg19156968
hg18156968
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1051972
Supporting Variants
Samples
Known GenesSLC2A14, SLC2A3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3521920
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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