A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16285818



Internal ID20495036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:8677133..8678918hg38UCSC Ensembl
chr3:8718819..8720604hg19UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg381786
hg191786
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4737761
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16285818
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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