A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18144660



Internal ID20711700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:82580274..82915321hg38UCSC Ensembl
chr6:83289991..83625040hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg38335048
hg19335050
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6414715
Supporting Variants
Samples
Known GenesUBE3D
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18144660
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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