A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2751059



Internal ID12637925
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:31086666..31253973hg38UCSC Ensembl
Innerchr12:31239600..31406907hg19UCSC Ensembl
Innerchr12:31130867..31298174hg18UCSC Ensembl
Innerchr12:31130867..31298174hg17UCSC Ensembl
Cytoband12p11.21
Allele length
AssemblyAllele length
hg38167308
hg19167308
hg18167308
hg17167308
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv62e55
Supporting Variantsessv6985116, essv6987160, essv6985115
SamplesSPC_10
Known GenesDDX11
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)esv2751059
Frequency
Sample Size771
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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