A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5941648



Internal ID22717076
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:23746939..23750790hg38UCSC Ensembl
chr15:23992086..23995937hg19UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg383852
hg193852
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17375491
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5941648
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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