A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6065463



Internal ID21974696
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:25988555..25988555hg38UCSC Ensembl
chr4:25990177..25990177hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg38459
hg19459
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17546332
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6065463
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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