A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5899296



Internal ID22674425
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:47056814..47275173hg38UCSC Ensembl
chr3:47098304..47316663hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg38218360
hg19218360
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17414373
Samples
Known GenesKIF9, KIF9-AS1, SETD2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5899296
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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