A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5497185



Internal ID274233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:22987635..22987902hg38UCSC Ensembl
chr14:23456844..23457111hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38268
hg19268
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17693947
Samples
Known GenesC14orf93
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5497185
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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