A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3627090



Internal ID7013920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:86510299..86542779hg38UCSC Ensembl
Innerchr11:86510342..86542737hg38UCSC Ensembl
Outerchr11:86510257..86542822hg38UCSC Ensembl
chr11:86221341..86253821hg19UCSC Ensembl
Innerchr11:86221384..86253779hg19UCSC Ensembl
Outerchr11:86221299..86253864hg19UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg3832481
hg1932481
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14221923
SamplesHG03078
Known GenesME3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3627090
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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