A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3627553



Internal ID7014381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:103363023..103433489hg38UCSC Ensembl
Innerchr11:103363041..103433472hg38UCSC Ensembl
Outerchr11:103363006..103433507hg38UCSC Ensembl
chr11:103233751..103304217hg19UCSC Ensembl
Innerchr11:103233769..103304200hg19UCSC Ensembl
Outerchr11:103233734..103304235hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg3870467
hg1970467
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14258066
SamplesHG01531
Known GenesDYNC2H1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3627553
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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