A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5888965



Internal ID22663975
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:21416005..21416327hg38UCSC Ensembl
chr3:21457497..21457819hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg38323
hg19323
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17420907
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5888965
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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