A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14945258



Internal ID3765225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:25665855..25667420hg38UCSC Ensembl
Innerchr14:25665861..25667415hg38UCSC Ensembl
Outerchr14:25665850..25667426hg38UCSC Ensembl
chr14:26135061..26136626hg19UCSC Ensembl
Innerchr14:26135067..26136621hg19UCSC Ensembl
Outerchr14:26135056..26136632hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg381566
hg191566
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3633835
Supporting Variants
SamplesHG03394
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14945258
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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