A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4751821



Internal ID20527681
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 StatusM
Merged Variants
Supporting Variantsnssv16263056
Samples
Known GenesLPCAT3
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4751821
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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