A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17692617



Internal ID116283
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:99984564..99984784hg38UCSC Ensembl
chr13:100636818..100637038hg19UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg38221
hg19221
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5504483
Supporting Variants
Samples
Known GenesZIC2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17692617
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