A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17425334



Internal ID22483204
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:97781298..97781348hg38UCSC Ensembl
chr3:97500142..97500192hg19UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5901978
Supporting Variants
Samples
Known GenesARL6
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17425334
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