A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17699491



Internal ID123157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:92873252..92874382hg38UCSC Ensembl
chr14:93339597..93340727hg19UCSC Ensembl
Cytoband14q32.12
Allele length
AssemblyAllele length
hg381131
hg191131
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5507498
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17699491
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.004215


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