A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2661487



Internal ID9927592
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:35365164..35366581hg38UCSC Ensembl
chr6:35332941..35334358hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg381418
hg191418
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6176708, essv5778924, essv6054488, essv6580112, essv5996515, essv5475449, essv6162395, essv5965399, essv6218139, essv5533432, essv5719739, essv6413254, essv5596812, essv5627944, essv6471337, essv6444810, essv6533078, essv6281953, essv6008489, essv5738038, essv5701581
SamplesNA19394, NA19700, NA19359, NA18510, NA19138, NA18498, NA18868, HG01440, NA18908, NA18867, NA19451, HG01183, NA19247, NA19462, NA19391, NA19982, NA18499, NA18856, NA19395, NA19439, NA19713
Known GenesPPARD
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2661487
Frequency
Sample Size1151
Observed Gain0
Observed Loss21
Observed Complex0
Frequencyn/a


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