A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3625664



Internal ID7012498
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:24213175..24263777hg38UCSC Ensembl
chr11:24234721..24285323hg19UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg3850603
hg1950603
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14058307, essv14058308, essv14058309
SamplesHG02040, HG02364, HG02410
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3625664
Frequency
Sample Size2504
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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