A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17601616



Internal ID21793663
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:89193623..89193623hg38UCSC Ensembl
chr12:89587400..89587400hg19UCSC Ensembl
Cytoband12q21.33
Allele length
AssemblyAllele length
hg38332
hg19332
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6086934
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17601616
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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