A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3635527



Internal ID7022326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:101357008..101360105hg38UCSC Ensembl
Innerchr14:101357045..101360068hg38UCSC Ensembl
Outerchr14:101356971..101360142hg38UCSC Ensembl
chr14:101823345..101826442hg19UCSC Ensembl
Innerchr14:101823382..101826405hg19UCSC Ensembl
Outerchr14:101823308..101826479hg19UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg383098
hg193098
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15108807
SamplesHG03743
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3635527
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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