A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14243297



Internal ID3364372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:95188025..95189459hg38UCSC Ensembl
Innerchr11:95188057..95189427hg38UCSC Ensembl
Outerchr11:95187993..95189491hg38UCSC Ensembl
chr11:94921189..94922623hg19UCSC Ensembl
Innerchr11:94921221..94922591hg19UCSC Ensembl
Outerchr11:94921157..94922655hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg381435
hg191435
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3627339
Supporting Variants
SamplesHG03016
Known GenesSESN3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14243297
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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