A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3611651



Internal ID6651869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:167156028..167313697hg38UCSC Ensembl
chr6:167569516..167727185hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38157670
hg19157670
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1240e214
Supporting Variantsessv12643396, essv12643397
SamplesNA12004, HG03518
Known GenesGPR31, TCP10L2, UNC93A
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3611651
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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