A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5937420



Internal ID22712787
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 StatusM
Merged Variants
Supporting Variantsnssv17388159
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5937420
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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