A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16282921



Internal ID20492139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:112747845..112747845hg38UCSC Ensembl
chr3:112466692..112466692hg19UCSC Ensembl
Cytoband3q13.2
Allele length
AssemblyAllele length
hg383144
hg193144
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4767044
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16282921
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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