A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3626129



Internal ID7012963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:42875552..42882513hg38UCSC Ensembl
chr11:42897102..42904063hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg386962
hg196962
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14111583, essv14111582, essv14111584
SamplesHG01456, HG01140, HG03343
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3626129
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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