A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2661116



Internal ID9580535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:161394265..161439021hg38UCSC Ensembl
chr6:161815297..161860053hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3844757
hg1944757
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5980908, essv6359179, essv6559307, essv6322106, essv6463000
SamplesNA19355, NA19448, NA19383, NA19462, NA19375
Known GenesPARK2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2661116
Frequency
Sample Size1151
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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