A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13992150



Internal ID3993966
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3625086
Supporting Variants
SamplesHG00629
Known GenesCHID1, TSPAN4
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13992150
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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