A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17607319



Internal ID21799366
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:25462703..25462703hg38UCSC Ensembl
chr12:25615637..25615637hg19UCSC Ensembl
Cytoband12p12.1
Allele length
AssemblyAllele length
hg382698
hg192698
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6085919
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17607319
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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