A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3626814



Internal ID7013644
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:73442828..73445436hg38UCSC Ensembl
Innerchr11:73442830..73445434hg38UCSC Ensembl
Outerchr11:73442826..73445438hg38UCSC Ensembl
chr11:73153873..73156481hg19UCSC Ensembl
Innerchr11:73153875..73156479hg19UCSC Ensembl
Outerchr11:73153871..73156483hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg382609
hg192609
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14212173
SamplesHG02799
Known GenesFAM168A
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3626814
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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