A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17388159



Internal ID22446029
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:26308849..26394466hg38UCSC Ensembl
chr15:26553996..26639613hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg3885618
hg1985618
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5937420
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17388159
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001


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