A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4759879



Internal ID20535739
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:52269157..52269157hg38UCSC Ensembl
chr12:52662941..52662941hg19UCSC Ensembl
Cytoband12q13.13
Allele length
AssemblyAllele length
hg38266
hg19266
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16294044
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4759879
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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