A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17696170



Internal ID119836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:51272910..51279514hg38UCSC Ensembl
chr14:51739628..51746232hg19UCSC Ensembl
Cytoband14q22.1
Allele length
AssemblyAllele length
hg386605
hg196605
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5498431
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17696170
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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