A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2669124



Internal ID9935229
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:47819584..47821920hg38UCSC Ensembl
Outerchr11:47819547..47821970hg38UCSC Ensembl
Innerchr11:47841136..47843472hg19UCSC Ensembl
Outerchr11:47841099..47843522hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg382424
hg192424
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5923502
SamplesNA18949
Known GenesNUP160
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2669124
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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