A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15193353



Internal ID21332241
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:116599211..116599211hg38UCSC Ensembl
chr12:117037016..117037016hg19UCSC Ensembl
Cytoband12q24.22
Allele length
AssemblyAllele length
hg38343
hg19343
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3931362
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15193353
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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