A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6355605



Internal ID21013158
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:80516630..80576906hg38UCSC Ensembl
chr3:80565780..80626056hg19UCSC Ensembl
Cytoband3p12.2
Allele length
AssemblyAllele length
hg3860277
hg1960277
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18209428
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6355605
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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