A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3506167



Internal ID18804448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:7818125..7927734hg38UCSC Ensembl
Innerchr12:7970721..8080330hg19UCSC Ensembl
Innerchr12:7861988..7971597hg18UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg38109610
hg19109610
hg18109610
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1040774
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)nssv3506167
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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