A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17602142



Internal ID21794189
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:120953152..120961373hg38UCSC Ensembl
chr12:121390955..121399176hg19UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg388222
hg198222
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6020559
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17602142
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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