A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6356763



Internal ID21014316
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:186742749..186764716hg38UCSC Ensembl
chr3:186460538..186482505hg19UCSC Ensembl
Cytoband3q27.3
Allele length
AssemblyAllele length
hg3821968
hg1921968
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18212214
Samples
Known GenesKNG1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6356763
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