A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13269783



Internal ID3271599
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:102532605..102572593hg38UCSC Ensembl
chr8:103544833..103584821hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg3839989
hg1939989
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3618224
Supporting Variants
SamplesHG03021
Known GenesODF1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13269783
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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