A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3626714



Internal ID7013544
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:67589766..67596623hg38UCSC Ensembl
Innerchr11:67589777..67596612hg38UCSC Ensembl
Outerchr11:67589755..67596634hg38UCSC Ensembl
chr11:67357237..67364094hg19UCSC Ensembl
Innerchr11:67357248..67364083hg19UCSC Ensembl
Outerchr11:67357226..67364105hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg386858
hg196858
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14197583
SamplesHG02522
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3626714
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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