A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6400036



Internal ID21057589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:36194101..36197400hg38UCSC Ensembl
chr6:36161878..36165177hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg383300
hg193300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18230323
Samples
Known GenesBRPF3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6400036
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