A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5892436



Internal ID22667487
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:145502164..145538252hg38UCSC Ensembl
chr3:145219951..145256039hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg3836089
hg1936089
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17391195
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5892436
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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