A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2669522



Internal ID9588941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:162194353..162206638hg38UCSC Ensembl
chr6:162615385..162627670hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3812286
hg1912286
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5641072
SamplesNA19703
Known GenesPARK2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2669522
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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