A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3625561



Internal ID7012395
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:20876987..20913391hg38UCSC Ensembl
chr11:20898533..20934937hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3836405
hg1936405
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14047455
SamplesHG02384
Known GenesNELL1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3625561
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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