A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2664415



Internal ID9583834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:161815919..161848972hg38UCSC Ensembl
Outerchr6:161815882..161849022hg38UCSC Ensembl
Innerchr6:162236951..162270004hg19UCSC Ensembl
Outerchr6:162236914..162270054hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3833141
hg1933141
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6546828
SamplesNA20754
Known GenesPARK2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2664415
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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