A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17610330



Internal ID21802377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:41453906..41453906hg38UCSC Ensembl
chr12:41847708..41847708hg19UCSC Ensembl
Cytoband12q12
Allele length
AssemblyAllele length
hg38228
hg19228
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6090849
Supporting Variants
Samples
Known GenesPDZRN4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17610330
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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