A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3627391



Internal ID7014220
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:96976376..97076553hg38UCSC Ensembl
Innerchr11:96976399..97076531hg38UCSC Ensembl
Outerchr11:96976354..97076576hg38UCSC Ensembl
chr11:96847376..96947553hg19UCSC Ensembl
Innerchr11:96847399..96947531hg19UCSC Ensembl
Outerchr11:96847354..96947576hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg38100178
hg19100178
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14245417
SamplesHG02952
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3627391
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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