A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5933764



Internal ID22709080
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:83782235..83791056hg38UCSC Ensembl
chr15:84450987..84459808hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg388822
hg198822
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17384437
Samples
Known GenesADAMTSL3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5933764
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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