A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5905201



Internal ID22680385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:161864316..161864382hg38UCSC Ensembl
chr3:161582104..161582170hg19UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17410906
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5905201
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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