A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3626859



Internal ID7013689
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:75646837..75648527hg38UCSC Ensembl
Innerchr11:75646841..75648523hg38UCSC Ensembl
Outerchr11:75646833..75648531hg38UCSC Ensembl
chr11:75357882..75359572hg19UCSC Ensembl
Innerchr11:75357886..75359568hg19UCSC Ensembl
Outerchr11:75357878..75359576hg19UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg381691
hg191691
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14214049
SamplesNA19213
Known GenesMAP6
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3626859
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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