A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17696486



Internal ID120152
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:35426928..35429272hg38UCSC Ensembl
chr14:35896134..35898478hg19UCSC Ensembl
Cytoband14q13.2
Allele length
AssemblyAllele length
hg382345
hg192345
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5504079
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17696486
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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