A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5898352



Internal ID22673465
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:112201698..112201893hg38UCSC Ensembl
chr3:111920545..111920740hg19UCSC Ensembl
Cytoband3q13.2
Allele length
AssemblyAllele length
hg38196
hg19196
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17405047
Samples
Known GenesSLC9C1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5898352
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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