A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17697697



Internal ID121363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:94948637..94953713hg38UCSC Ensembl
chr14:95414974..95420050hg19UCSC Ensembl
Cytoband14q32.13
Allele length
AssemblyAllele length
hg385077
hg195077
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5501634
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17697697
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.01385


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