A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17699278



Internal ID122944
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:74251215..74252775hg38UCSC Ensembl
chr14:74717918..74719478hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg381561
hg191561
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5510521
Supporting Variants
Samples
Known GenesVSX2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17699278
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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