A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4748946



Internal ID20524974
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:161917693..161917879hg38UCSC Ensembl
chr3:161635481..161635667hg19UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg38187
hg19187
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16268639
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4748946
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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