A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5900796



Internal ID22675942
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:155761843..155795689hg38UCSC Ensembl
chr3:155479632..155513478hg19UCSC Ensembl
Cytoband3q25.31
Allele length
AssemblyAllele length
hg3833847
hg1933847
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17418560
Samples
Known GenesC3orf33
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5900796
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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