A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3625086



Internal ID6665238
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:860117..882352hg38UCSC Ensembl
chr11:860117..882352hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3822236
hg1922236
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13992150
SamplesHG00629
Known GenesCHID1, TSPAN4
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3625086
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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