A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3633811



Internal ID7020617
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:24675077..24693168hg38UCSC Ensembl
chr14:25144283..25162374hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3818092
hg1918092
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14942631
SamplesHG04047
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3633811
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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