A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3633861



Internal ID7020667
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:26927576..26947225hg38UCSC Ensembl
Innerchr14:26927576..26947225hg38UCSC Ensembl
Outerchr14:26927336..26947529hg38UCSC Ensembl
chr14:27396782..27416431hg19UCSC Ensembl
Innerchr14:27396782..27416431hg19UCSC Ensembl
Outerchr14:27396542..27416735hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3819650
hg1919650
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14946917
SamplesHG00260
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3633861
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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