A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17602707



Internal ID21794754
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:41801253..41801253hg38UCSC Ensembl
chr12:42195055..42195055hg19UCSC Ensembl
Cytoband12q12
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6096446
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17602707
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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