A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6360018



Internal ID21017571
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:94705555..94879762hg38UCSC Ensembl
chr3:94424399..94598606hg19UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg38174208
hg19174208
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18210802
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6360018
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer