A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2661551



Internal ID9927656
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:19143056..19156984hg38UCSC Ensembl
chr9:19143054..19156982hg19UCSC Ensembl
Cytoband9p22.1
Allele length
AssemblyAllele length
hg3813929
hg1913929
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6179825
SamplesNA18952
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2661551
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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