A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3634098



Internal ID7020902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:37758365..37759048hg38UCSC Ensembl
Innerchr14:37758389..37759024hg38UCSC Ensembl
Outerchr14:37758341..37759072hg38UCSC Ensembl
chr14:38227570..38228253hg19UCSC Ensembl
Innerchr14:38227594..38228229hg19UCSC Ensembl
Outerchr14:38227546..38228277hg19UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg38684
hg19684
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14970163
SamplesHG02724
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3634098
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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