A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17483765



Internal ID22541672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:111573188..111575787hg38UCSC Ensembl
chr3:111292035..111294634hg19UCSC Ensembl
Cytoband3q13.13
Allele length
AssemblyAllele length
hg382600
hg192600
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5834279
Supporting Variants
Samples
Known GenesCD96
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17483765
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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