A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2661667



Internal ID9927772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:136949064..136954870hg38UCSC Ensembl
Outerchr9:136948693..136955240hg38UCSC Ensembl
Innerchr9:139843516..139849322hg19UCSC Ensembl
Outerchr9:139843145..139849692hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg386548
hg196548
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5759711, essv5696977, essv6467314, essv5490887, essv5542761, essv5571006, essv6014413, essv5876182, essv5454998, essv5440093, essv6103524, essv5685376, essv5433754, essv6016802, essv6113949, essv6261044, essv5966522, essv6110517, essv5639032, essv6555299, essv6303723, essv6133979, essv5717662, essv5897258, essv5831132, essv6294667, essv5441342, essv6384163
SamplesHG01060, HG01052, HG01079, HG01188, HG01051, HG01070, HG01167, HG01069, HG01080, HG01072, HG01198, HG01183, HG01187, HG01171, HG01095, HG01102, HG01197, HG01182, HG01101, HG01107, HG01204, HG01075, HG01190, HG00734, HG00638, HG01055, HG01191, HG01061
Known GenesLCN12
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2661667
Frequency
Sample Size1151
Observed Gain0
Observed Loss28
Observed Complex0
Frequencyn/a


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