A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14979175



Internal ID6851063
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:39894626..39910608hg38UCSC Ensembl
chr14:40363830..40379812hg19UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg3815983
hg1915983
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3634161
Supporting Variants
SamplesNA21087
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14979175
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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