A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2669165



Internal ID9935270
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:152905617..152906604hg38UCSC Ensembl
chr6:153226752..153227739hg19UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg38988
hg19988
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6343548, essv6159462, essv5517145, essv6361232, essv6093129, essv6330705, essv6548131, essv6465956, essv6029969, essv6296906, essv6066749, essv6027567, essv6145678, essv6183959, essv5842129, essv6209854, essv5598237, essv5616002, essv5489933
SamplesNA18508, NA19443, NA19448, NA19313, NA19462, NA19236, NA18499, NA19453, NA18853, HG01148, NA19440, NA19147, NA19434, NA19444, HG01174, NA19334, NA19470, NA19468, NA19474
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2669165
Frequency
Sample Size1151
Observed Gain0
Observed Loss19
Observed Complex0
Frequencyn/a


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