A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4764965



Internal ID20540825
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:141272543..141272543hg38UCSC Ensembl
chr3:140991385..140991385hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg38179
hg19179
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16264552
Samples
Known GenesACPL2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4764965
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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