A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3625869



Internal ID7012703
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:32994194..33026435hg38UCSC Ensembl
chr11:33015740..33047981hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg3832242
hg1932242
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14085168
SamplesHG02058
Known GenesDEPDC7
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3625869
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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