A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3611661



Internal ID6998567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:167350999..167512302hg38UCSC Ensembl
chr6:167764487..167924494hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38161304
hg19160008
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12643456
SamplesHG03518
Known GenesTCP10
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3611661
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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