A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2666264



Internal ID9932369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:2568232..2570788hg38UCSC Ensembl
Outerchr6:2567861..2571158hg38UCSC Ensembl
Innerchr6:2568466..2571022hg19UCSC Ensembl
Outerchr6:2568095..2571392hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg383298
hg193298
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1069e199
Supporting Variantsessv5958265, essv5459282, essv6110429, essv5452486, essv6126650, essv5554895, essv5449517, essv6566065, essv5598714, essv6001094, essv5850513, essv6459912, essv6308007, essv6459696, essv6370525, essv5519863, essv6386136, essv6101339, essv6126492, essv6087957, essv5598669, essv5800275, essv6579248, essv5750794, essv6411879, essv5714160, essv6413886
SamplesNA18924, NA19204, NA18508, NA18917, NA18504, NA18510, NA18519, NA18489, NA19131, NA18916, NA19138, NA18498, NA18874, NA19189, NA19209, NA19200, NA18933, NA19236, NA18499, NA18912, NA19225, NA18523, NA18909, NA19248, NA18873, NA19116, NA18511
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2666264
Frequency
Sample Size1151
Observed Gain0
Observed Loss27
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer