A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3633842



Internal ID7020648
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:26232281..26239065hg38UCSC Ensembl
Innerchr14:26232281..26239065hg38UCSC Ensembl
Outerchr14:26231781..26239565hg38UCSC Ensembl
chr14:26701487..26708271hg19UCSC Ensembl
Innerchr14:26701487..26708271hg19UCSC Ensembl
Outerchr14:26700987..26708771hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg386785
hg196785
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14946640
SamplesHG01360
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3633842
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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