A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5992998



Internal ID21902341
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:196511185..196511295hg38UCSC Ensembl
chr3:196238056..196238166hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg38111
hg19111
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17542211
Samples
Known GenesC3orf43
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5992998
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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