A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6022518



Internal ID21931861
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:38799622..38802583hg38UCSC Ensembl
chr12:39193424..39196385hg19UCSC Ensembl
Cytoband12q12
Allele length
AssemblyAllele length
hg382962
hg192962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17609793
Samples
Known GenesCPNE8
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6022518
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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