A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2664671



Internal ID9584090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:167129527..167130932hg38UCSC Ensembl
chr6:167543015..167544420hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg381406
hg191406
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5924432, essv5966119, essv5660595, essv6510683, essv5942771, essv5726303, essv5531221, essv6190426, essv5622476, essv6271829, essv5427066, essv5564092, essv5420804, essv5768062, essv6389221, essv5515399, essv6418129, essv5935602, essv6208984, essv5572274, essv5443040, essv6214148, essv5583475, essv5843847, essv5396037
SamplesNA19445, NA19404, NA19437, NA19114, NA18874, NA19223, NA19453, NA19920, NA19236, NA19467, NA19982, NA19429, NA18916, NA19247, NA19129, NA19393, NA18498, NA18486, NA19657, NA19909, NA18910, NA18907, NA19116, NA19350, NA18908
Known GenesCCR6
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2664671
Frequency
Sample Size1151
Observed Gain0
Observed Loss25
Observed Complex0
Frequencyn/a


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