A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5508496



Internal ID285184
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:22771920..22772303hg38UCSC Ensembl
chr14:23241129..23241512hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38384
hg19384
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17693930
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5508496
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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