A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6414565



Internal ID21072118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:21428822..21450377hg38UCSC Ensembl
chr6:21429053..21450608hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg3821556
hg1921556
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18235861
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6414565
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