A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5898068



Internal ID22673179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:152589134..152589366hg38UCSC Ensembl
chr3:152306923..152307155hg19UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg38233
hg19233
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17423773
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5898068
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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