A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5900828



Internal ID22675975
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:104925173..104929997hg38UCSC Ensembl
chr3:104644017..104648841hg19UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg384825
hg194825
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17407769
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5900828
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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