A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2664189



Internal ID9930294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:73614658..73622114hg38UCSC Ensembl
Outerchr10:73614287..73622484hg38UCSC Ensembl
Innerchr10:75374416..75381872hg19UCSC Ensembl
Outerchr10:75374045..75382242hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg388198
hg198198
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv155e199
Supporting Variantsessv6365342, essv5862083, essv6426467, essv5907390, essv5400419, essv5816709, essv5903064, essv5538108, essv6573166, essv5830340, essv6515528, essv6575364, essv6314833, essv5730753, essv5538767, essv6063729, essv6537963, essv6471329, essv5636877, essv5409078, essv5909586, essv5854099, essv6136234, essv6346063, essv6461742
SamplesNA18502, NA18924, NA18508, NA18504, NA19190, NA19107, NA18916, NA19138, NA18498, NA19172, NA19189, NA18910, NA18871, NA19114, NA18499, NA19099, NA18523, NA19108, NA18517, NA18501, NA19093, NA19102, NA18505, NA19129, NA18511
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2664189
Frequency
Sample Size1151
Observed Gain0
Observed Loss25
Observed Complex0
Frequencyn/a


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