A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6020814



Internal ID21930157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:41281062..41281408hg38UCSC Ensembl
chr12:41674864..41675210hg19UCSC Ensembl
Cytoband12q12
Allele length
AssemblyAllele length
hg38347
hg19347
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17607294
Samples
Known GenesPDZRN4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6020814
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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