A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5901250



Internal ID22676399
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:76883901..76893337hg38UCSC Ensembl
chr3:76933052..76942488hg19UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg389437
hg199437
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17418079
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5901250
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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