A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17431973



Internal ID22489844
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:102967973..102968297hg38UCSC Ensembl
chr8:103980201..103980525hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg38325
hg19325
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5913794
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17431973
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