A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2669436



Internal ID9935541
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:85858556..85861255hg38UCSC Ensembl
chr9:88473471..88476170hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg382700
hg192700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6134092, essv6544731, essv5552748, essv5866953, essv6283121, essv6080992, essv6324166, essv6540528, essv6192695, essv6312114, essv5481271, essv6463210, essv6302350, essv5560637, essv6423160, essv5546290, essv6500544, essv6486134, essv6234447, essv5699522, essv5437560, essv6489920, essv6095248, essv5459076, essv5433896
SamplesNA18924, NA19909, NA18486, NA20332, NA19374, NA19373, NA19404, NA18874, NA19137, NA19238, NA19189, NA19445, NA19403, NA19347, NA18907, NA18499, NA19453, NA18853, NA19625, NA19436, NA19834, NA19712, NA19434, NA19711, NA19129
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2669436
Frequency
Sample Size1151
Observed Gain0
Observed Loss25
Observed Complex0
Frequencyn/a


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