A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17608049



Internal ID21800096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:111735064..111735179hg38UCSC Ensembl
chr12:112172868..112172983hg19UCSC Ensembl
Cytoband12q24.12
Allele length
AssemblyAllele length
hg38116
hg19116
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6024494
Supporting Variants
Samples
Known GenesACAD10
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17608049
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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