A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2751117



Internal ID12984669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:7864877..7989987hg38UCSC Ensembl
Innerchr12:8017473..8142583hg19UCSC Ensembl
Innerchr12:7908740..8033850hg18UCSC Ensembl
Innerchr12:7908740..8033850hg17UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg38125111
hg19125111
hg18125111
hg17125111
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv59e55
Supporting Variantsessv6985415, essv6980805
SamplesBEC_175
Known GenesSLC2A14, SLC2A3
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
CommentsSample level SV from stringent call set
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)esv2751117
Frequency
Sample Size771
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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