A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4763765



Internal ID20539625
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:16412786..16412786hg38UCSC Ensembl
chr10:16454785..16454785hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16259998
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4763765
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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