A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13285705



Internal ID3688020
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:110614349..110652004hg38UCSC Ensembl
chr8:111626578..111664233hg19UCSC Ensembl
Cytoband8q23.2
Allele length
AssemblyAllele length
hg3837656
hg1937656
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3618400
Supporting Variants
SamplesHG03295
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13285705
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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