A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3634422



Internal ID7021225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:47944703..47964855hg38UCSC Ensembl
Innerchr14:47945203..47964355hg38UCSC Ensembl
Outerchr14:47943703..47965855hg38UCSC Ensembl
chr14:48413906..48434058hg19UCSC Ensembl
Innerchr14:48414406..48433558hg19UCSC Ensembl
Outerchr14:48412906..48435058hg19UCSC Ensembl
Cytoband14q21.3
Allele length
AssemblyAllele length
hg3820153
hg1920153
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15004533
SamplesHG03172
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3634422
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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