A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4762713



Internal ID20538573
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:55586543..55586543hg38UCSC Ensembl
chr16:55620455..55620455hg19UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16295231
Samples
Known GenesLPCAT2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4762713
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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