A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5933638



Internal ID22708952
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:37660529..37661560hg38UCSC Ensembl
chr15:37952730..37953761hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg381032
hg191032
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17385383
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5933638
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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