A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17601919



Internal ID21793966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:115915509..115915509hg38UCSC Ensembl
chr12:116353314..116353314hg19UCSC Ensembl
Cytoband12q24.21
Allele length
AssemblyAllele length
hg38311
hg19311
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6084183
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17601919
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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