A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17693902



Internal ID117568
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:22449124..22531939hg38UCSC Ensembl
chr14:22918116..23000889hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3882816
hg1982774
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5511461
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17693902
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00328


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