A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16286939



Internal ID20496157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:161949453..161997079hg38UCSC Ensembl
chr3:161667241..161714867hg19UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg3847627
hg1947627
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4749569
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16286939
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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