A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3625812



Internal ID7012646
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:30102975..30110334hg38UCSC Ensembl
Innerchr11:30102988..30110322hg38UCSC Ensembl
Outerchr11:30102963..30110347hg38UCSC Ensembl
chr11:30124522..30131881hg19UCSC Ensembl
Innerchr11:30124535..30131869hg19UCSC Ensembl
Outerchr11:30124510..30131894hg19UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg387360
hg197360
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14078299
SamplesNA12748
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3625812
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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