A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17698853



Internal ID122519
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:101556234..101557963hg38UCSC Ensembl
chr14:102022571..102024300hg19UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg381730
hg191730
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5511362
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17698853
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000624


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