A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6078304



Internal ID21987537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:32826695..32826695hg38UCSC Ensembl
chr5:32826801..32826801hg19UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17551517
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6078304
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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