A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5898965



Internal ID22674090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:36923389..36923523hg38UCSC Ensembl
chr3:36964880..36965014hg19UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg38135
hg19135
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17426115
Samples
Known GenesTRANK1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5898965
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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