A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17352720



Internal ID22578389
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:79472008..79474200hg38UCSC Ensembl
chr10:81231764..81233956hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg382193
hg192193
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5916370
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17352720
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001


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