A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3626697



Internal ID7013528
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:66571567..66573559hg38UCSC Ensembl
Innerchr11:66571617..66573509hg38UCSC Ensembl
Outerchr11:66571517..66573609hg38UCSC Ensembl
chr11:66339038..66341030hg19UCSC Ensembl
Innerchr11:66339088..66340980hg19UCSC Ensembl
Outerchr11:66338988..66341080hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg381993
hg191993
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14195780, essv14195781
SamplesHG02026, HG01841
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3626697
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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