A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5500065



Internal ID277011
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:95516543..95516834hg38UCSC Ensembl
chr14:95982880..95983171hg19UCSC Ensembl
Cytoband14q32.13
Allele length
AssemblyAllele length
hg38292
hg19292
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17698642
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5500065
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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