A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14869343



Internal ID3771262
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:96880811..96884866hg38UCSC Ensembl
Innerchr13:96880820..96884857hg38UCSC Ensembl
Outerchr13:96880802..96884875hg38UCSC Ensembl
chr13:97533065..97537120hg19UCSC Ensembl
Innerchr13:97533074..97537111hg19UCSC Ensembl
Outerchr13:97533056..97537129hg19UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg384056
hg194056
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3633282
Supporting Variants
SamplesHG03401
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14869343
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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