A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5897100



Internal ID22672198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:152800983..152801463hg38UCSC Ensembl
chr3:152518772..152519252hg19UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg38481
hg19481
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17428900
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5897100
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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