A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17613273



Internal ID21805320
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:104174351..104174351hg38UCSC Ensembl
chr12:104568129..104568129hg19UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6081064
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17613273
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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