A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17612295



Internal ID21804342
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:92473119..92473119hg38UCSC Ensembl
chr12:92866895..92866895hg19UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6093048
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17612295
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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