A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5496872



Internal ID273938
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:96061029..96069361hg38UCSC Ensembl
chr14:96527366..96535698hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg388333
hg198333
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17698672
Samples
Known GenesC14orf132
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5496872
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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