A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17386492



Internal ID22444362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:30892411..30892495hg38UCSC Ensembl
chr15:31184614..31184698hg19UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg3885
hg1985
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5944668
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17386492
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.003


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