A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16263056



Internal ID20472274
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:6999998..6999998hg38UCSC Ensembl
chr12:7108090..7108090hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg38755
hg19755
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4751821
Supporting Variants
Samples
Known GenesLPCAT3
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16263056
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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