A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15086742



Internal ID2059977
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:84434665..84450193hg38UCSC Ensembl
chr14:84901009..84916537hg19UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg3815529
hg1915529
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3635161
Supporting Variants
SamplesHG01879
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15086742
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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