A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17445862



Internal ID22503732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:79466501..79467748hg38UCSC Ensembl
chr9:82081416..82082663hg19UCSC Ensembl
Cytoband9q21.31
Allele length
AssemblyAllele length
hg381248
hg191248
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5925534
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17445862
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