A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17401487



Internal ID22459357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:183742914..183797308hg38UCSC Ensembl
chr2:184607641..184662035hg19UCSC Ensembl
Cytoband2q32.1
Allele length
AssemblyAllele length
hg3854395
hg1954395
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5887824
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17401487
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