A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14949887



Internal ID4028205
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:27990251..28053436hg38UCSC Ensembl
chr14:28459457..28522642hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3863186
hg1963186
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3633895
Supporting Variants
SamplesHG03681
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14949887
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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