A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3625832



Internal ID6665980
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:31532359..31582371hg38UCSC Ensembl
chr11:31553906..31603918hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg3850013
hg1950013
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14079501
SamplesHG01447
Known GenesELP4
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3625832
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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