A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5894294



Internal ID22669366
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:106923069..106928316hg38UCSC Ensembl
chr3:106641916..106647163hg19UCSC Ensembl
Cytoband3q13.12
Allele length
AssemblyAllele length
hg385248
hg195248
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17407139
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5894294
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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