A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3625454



Internal ID7012288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:16768992..16770601hg38UCSC Ensembl
Innerchr11:16768992..16770601hg38UCSC Ensembl
Outerchr11:16768628..16770841hg38UCSC Ensembl
chr11:16790539..16792148hg19UCSC Ensembl
Innerchr11:16790539..16792148hg19UCSC Ensembl
Outerchr11:16790175..16792388hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg381610
hg191610
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14036067, essv14036068, essv14036066
SamplesNA18543, HG00473, NA18612
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3625454
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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