A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6359526



Internal ID21017079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:70857500..70866434hg38UCSC Ensembl
chr3:70906651..70915585hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg388935
hg198935
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18208683
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6359526
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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