A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3627889



Internal ID7014714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:119243178..119245631hg38UCSC Ensembl
Innerchr11:119243192..119245618hg38UCSC Ensembl
Outerchr11:119243165..119245645hg38UCSC Ensembl
chr11:119113888..119116341hg19UCSC Ensembl
Innerchr11:119113902..119116328hg19UCSC Ensembl
Outerchr11:119113875..119116355hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg382454
hg192454
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14293352
SamplesHG00232
Known GenesCBL
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3627889
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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