A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6407982



Internal ID21065535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:63589823..63591236hg38UCSC Ensembl
chr6:64299728..64301141hg19UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg381414
hg191414
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18222178
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6407982
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