A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3618862



Internal ID7005744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:131716886..131868669hg38UCSC Ensembl
chr8:132729133..132880916hg19UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg38151784
hg19151784
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13334206
SamplesNA19921
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3618862
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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