A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6031508



Internal ID21940851
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:38797103..38800188hg38UCSC Ensembl
chr12:39190905..39193990hg19UCSC Ensembl
Cytoband12q12
Allele length
AssemblyAllele length
hg383086
hg193086
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17613818
Samples
Known GenesCPNE8
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6031508
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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