A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3631969



Internal ID7018779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:45762844..45778370hg38UCSC Ensembl
chr13:46336979..46352505hg19UCSC Ensembl
Cytoband13q14.13
Allele length
AssemblyAllele length
hg3815527
hg1915527
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14712210
SamplesHG01259
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3631969
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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