A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6104720



Internal ID22013953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:4225007..4225007hg38UCSC Ensembl
chr20:4205654..4205654hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg385953
hg195953
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17620143
Samples
Known GenesADRA1D
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6104720
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer