A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6419716



Internal ID21077269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:115148100..115186889hg38UCSC Ensembl
chr8:116160329..116199118hg19UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg3838790
hg1938790
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18218176
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6419716
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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