A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3627254



Internal ID7014084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:91618539..91700011hg38UCSC Ensembl
Innerchr11:91618570..91699980hg38UCSC Ensembl
Outerchr11:91618508..91700042hg38UCSC Ensembl
chr11:91351705..91433177hg19UCSC Ensembl
Innerchr11:91351736..91433146hg19UCSC Ensembl
Outerchr11:91351674..91433208hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg3881473
hg1981473
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14233476
SamplesHG01961
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3627254
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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