A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3631686



Internal ID7018494
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:30990707..30995552hg38UCSC Ensembl
chr13:31564844..31569689hg19UCSC Ensembl
Cytoband13q12.3
Allele length
AssemblyAllele length
hg384846
hg194846
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14682694
SamplesHG01119
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3631686
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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