A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14088610



Internal ID4090426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:34065737..34068115hg38UCSC Ensembl
Innerchr11:34065737..34068115hg38UCSC Ensembl
Outerchr11:34065529..34068319hg38UCSC Ensembl
chr11:34087284..34089662hg19UCSC Ensembl
Innerchr11:34087284..34089662hg19UCSC Ensembl
Outerchr11:34087076..34089866hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg382379
hg192379
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3625905
Supporting Variants
SamplesHG01808
Known GenesCAPRIN1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14088610
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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