A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2669042



Internal ID9935147
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:90233055..90236312hg38UCSC Ensembl
chr9:92995337..92998594hg19UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg383258
hg193258
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6190943, essv6354244
SamplesNA20760, HG01197
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2669042
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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