A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3627493



Internal ID7014322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:100732943..100744085hg38UCSC Ensembl
Innerchr11:100732980..100744049hg38UCSC Ensembl
Outerchr11:100732907..100744122hg38UCSC Ensembl
chr11:100603674..100614816hg19UCSC Ensembl
Innerchr11:100603711..100614780hg19UCSC Ensembl
Outerchr11:100603638..100614853hg19UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg3811143
hg1911143
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14250962, essv14250961
SamplesNA18946, HG03755
Known GenesARHGAP42
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3627493
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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