A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16934595



Internal ID23795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:59036775..59066841hg38UCSC Ensembl
chr3:59022501..59052567hg19UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg3830067
hg1930067
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5452372
Supporting Variants
Samples
Known GenesC3orf67
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16934595
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