A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17699050



Internal ID122716
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:81663061..81706428hg38UCSC Ensembl
chr14:82129405..82172772hg19UCSC Ensembl
Cytoband14q31.1
Allele length
AssemblyAllele length
hg3843368
hg1943368
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5503291
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17699050
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer