A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5897283



Internal ID22672384
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:111573692..111573749hg38UCSC Ensembl
chr3:111292539..111292596hg19UCSC Ensembl
Cytoband3q13.13
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17396900
Samples
Known GenesCD96
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5897283
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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