A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3627005



Internal ID6667153
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:82851491..82853001hg38UCSC Ensembl
Innerchr11:82851531..82852962hg38UCSC Ensembl
Outerchr11:82851452..82853041hg38UCSC Ensembl
chr11:82562533..82564043hg19UCSC Ensembl
Innerchr11:82562573..82564004hg19UCSC Ensembl
Outerchr11:82562494..82564083hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg381511
hg191511
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14219120
SamplesNA20894
Known GenesPRCP
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3627005
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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