A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2656549



Internal ID9575968
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:162075323..162085920hg38UCSC Ensembl
chr6:162496355..162506952hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3810598
hg1910598
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5738116, essv5395853
SamplesNA19338, NA19463
Known GenesPARK2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2656549
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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