A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17449390



Internal ID22507260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:113553619..113558053hg38UCSC Ensembl
chr8:114565848..114570282hg19UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg384435
hg194435
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5918035
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17449390
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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