A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3625431



Internal ID7012265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:15029801..15035222hg38UCSC Ensembl
Innerchr11:15029816..15035208hg38UCSC Ensembl
Outerchr11:15029787..15035237hg38UCSC Ensembl
chr11:15051347..15056768hg19UCSC Ensembl
Innerchr11:15051362..15056754hg19UCSC Ensembl
Outerchr11:15051333..15056783hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg385422
hg195422
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14034260
SamplesNA19001
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3625431
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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