A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5900533



Internal ID22675676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:141924072..141924366hg38UCSC Ensembl
chr3:141642914..141643208hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg38295
hg19295
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17390103
Samples
Known GenesATP1B3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5900533
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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