A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3611686



Internal ID6651904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:168158732..168252456hg38UCSC Ensembl
chr6:168559412..168653136hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3893725
hg1993725
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12645351
SamplesHG02678
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3611686
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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