A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2662124



Internal ID9581543
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:162157519..162159247hg38UCSC Ensembl
chr6:162578551..162580279hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg381729
hg191729
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6291854, essv6019069, essv5717709, essv5902868, essv5497596, essv5495088
SamplesNA19371, NA19451, NA18517, NA19248, NA19900, NA19346
Known GenesPARK2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2662124
Frequency
Sample Size1151
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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