A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17422823



Internal ID22480693
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:186311820..186312155hg38UCSC Ensembl
chr3:186029609..186029944hg19UCSC Ensembl
Cytoband3q27.3
Allele length
AssemblyAllele length
hg38336
hg19336
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5899117
Supporting Variants
Samples
Known GenesDGKG
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17422823
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