A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4752766



Internal ID20528626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:58315709..58315709hg38UCSC Ensembl
chr2:58542844..58542844hg19UCSC Ensembl
Cytoband2p16.1
Allele length
AssemblyAllele length
hg38400
hg19400
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16289212
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4752766
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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