A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6359436



Internal ID21016989
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:87340501..87347100hg38UCSC Ensembl
chr3:87389651..87396250hg19UCSC Ensembl
Cytoband3p11.2
Allele length
AssemblyAllele length
hg386600
hg196600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4942n223
Supporting Variantsnssv18210167
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6359436
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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