A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3634044



Internal ID7020848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:34893597..34905729hg38UCSC Ensembl
Innerchr14:34894097..34905229hg38UCSC Ensembl
Outerchr14:34892597..34906729hg38UCSC Ensembl
chr14:35362803..35374935hg19UCSC Ensembl
Innerchr14:35363303..35374435hg19UCSC Ensembl
Outerchr14:35361803..35375935hg19UCSC Ensembl
Cytoband14q13.2
Allele length
AssemblyAllele length
hg3812133
hg1912133
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14966167
SamplesNA19114
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3634044
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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