A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17389664



Internal ID22447534
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:165625863..165626154hg38UCSC Ensembl
chr2:166482373..166482664hg19UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg38292
hg19292
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5888779
Supporting Variants
Samples
Known GenesCSRNP3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17389664
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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