A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13150568



Internal ID3152384
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:27277090..27359993hg38UCSC Ensembl
chr8:27134607..27217510hg19UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg3882904
hg1982904
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3616717
Supporting Variants
SamplesNA19782
Known GenesPTK2B, TRIM35
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13150568
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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