A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17439403



Internal ID22497273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:101315752..101315831hg38UCSC Ensembl
chr8:102327980..102328059hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5911520
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17439403
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