A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2087n223



Internal ID22805055
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:30139601..30278800hg38UCSC Ensembl
chr14:30608807..30748006hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg38139200
hg19139200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6478748, nsv6491069, nsv6481317, nsv6479849, nsv6489779
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv2087n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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