A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3626812



Internal ID6666960
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:73213163..73237183hg38UCSC Ensembl
chr11:72924208..72948228hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg3824021
hg1924021
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14212168, essv14212169, essv14212167, essv14212170, essv14212171
SamplesHG02888, HG03246, HG03225, HG02819, NA19346
Known GenesP2RY2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3626812
Frequency
Sample Size2504
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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