A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14076676



Internal ID3621055
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:29518543..29526079hg38UCSC Ensembl
Innerchr11:29518565..29526057hg38UCSC Ensembl
Outerchr11:29518521..29526101hg38UCSC Ensembl
chr11:29540090..29547626hg19UCSC Ensembl
Innerchr11:29540112..29547604hg19UCSC Ensembl
Outerchr11:29540068..29547648hg19UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg387537
hg197537
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3625802
Supporting Variants
SamplesHG03212
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14076676
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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