A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3633992



Internal ID7020796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:32856255..32857131hg38UCSC Ensembl
Innerchr14:32856325..32857061hg38UCSC Ensembl
Outerchr14:32856185..32857201hg38UCSC Ensembl
chr14:33325461..33326337hg19UCSC Ensembl
Innerchr14:33325531..33326267hg19UCSC Ensembl
Outerchr14:33325391..33326407hg19UCSC Ensembl
Cytoband14q13.1
Allele length
AssemblyAllele length
hg38877
hg19877
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14959357, essv14959360, essv14959359, essv14959358
SamplesNA19068, HG01365, NA18986, NA18984
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3633992
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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