A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3611619



Internal ID6998525
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:165462035..165480247hg38UCSC Ensembl
chr6:165875523..165893735hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3818213
hg1918213
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12629998, essv12629997, essv12629999, essv12629996
SamplesHG03055, HG03136, NA19395, NA19144
Known GenesPDE10A
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3611619
Frequency
Sample Size2504
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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