A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3617211



Internal ID7004097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:52351443..52378368hg38UCSC Ensembl
chr8:53264003..53290928hg19UCSC Ensembl
Cytoband8q11.23
Allele length
AssemblyAllele length
hg3826926
hg1926926
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13200494
SamplesHG00559
Known GenesST18
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3617211
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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