A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15705346



Internal ID21377622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:41293027..41293224hg38UCSC Ensembl
chr12:41686829..41687026hg19UCSC Ensembl
Cytoband12q12
Allele length
AssemblyAllele length
hg38198
hg19198
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4390239
Supporting Variants
Samples
Known GenesPDZRN4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nssv15705346
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0402299


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