A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3626685



Internal ID7013516
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:65955847..65960643hg38UCSC Ensembl
Innerchr11:65955997..65960493hg38UCSC Ensembl
Outerchr11:65955697..65960793hg38UCSC Ensembl
chr11:65723318..65728114hg19UCSC Ensembl
Innerchr11:65723468..65727964hg19UCSC Ensembl
Outerchr11:65723168..65728264hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg384797
hg194797
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14193340
SamplesHG00537
Known GenesTSGA10IP
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3626685
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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