A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6031170



Internal ID21940513
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:122976084..122979060hg38UCSC Ensembl
chr12:123460631..123463607hg19UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg382977
hg192977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17609215
Samples
Known GenesOGFOD2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6031170
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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