A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3625088



Internal ID6665240
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:876861..979340hg38UCSC Ensembl
chr11:876861..979340hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg38102480
hg19102480
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13992154, essv13992155
SamplesHG00251, HG03830
Known GenesAP2A2, CHID1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3625088
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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