A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3611655



Internal ID6651873
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:167256381..167320502hg38UCSC Ensembl
chr6:167669869..167733990hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3864122
hg1964122
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12643423, essv12643422
SamplesHG02054, HG03518
Known GenesUNC93A
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3611655
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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