A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4760218



Internal ID20536078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:46892718..46892718hg38UCSC Ensembl
chr2:47119857..47119857hg19UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16295345
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4760218
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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