A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17608705



Internal ID21800752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:80180233..80180233hg38UCSC Ensembl
chr12:80574013..80574013hg19UCSC Ensembl
Cytoband12q21.31
Allele length
AssemblyAllele length
hg38155
hg19155
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6099151
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17608705
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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