A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18105966



Internal ID20673006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:85447993..85624878hg38UCSC Ensembl
chr3:85497143..85674028hg19UCSC Ensembl
Cytoband3p12.1
Allele length
AssemblyAllele length
hg38176886
hg19176886
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6369083
Supporting Variants
Samples
Known GenesCADM2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18105966
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