A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17437845



Internal ID22495715
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:54361455..54361514hg38UCSC Ensembl
chr8:55274015..55274074hg19UCSC Ensembl
Cytoband8q11.23
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5918889
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17437845
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.03


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