A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3626971



Internal ID7013801
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:81830232..82005098hg38UCSC Ensembl
chr11:81541274..81716140hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38174867
hg19174867
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14217904, essv14217905, essv14217903
SamplesNA21092, HG02561, NA12763
Known GenesMIR4300
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3626971
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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