A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17698669



Internal ID122335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:95994980..95998959hg38UCSC Ensembl
chr14:96461317..96465296hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg383980
hg193980
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5502199
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17698669
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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