A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17492201



Internal ID22550128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:98855499..98917853hg38UCSC Ensembl
chr3:98574343..98636697hg19UCSC Ensembl
Cytoband3q12.1
Allele length
AssemblyAllele length
hg3862355
hg1962355
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5837257
Supporting Variants
Samples
Known GenesDCBLD2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17492201
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