A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18040787



Internal ID20607827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:33222901..33224700hg38UCSC Ensembl
chr18:30802865..30804664hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg381800
hg191800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6531964
Supporting Variants
Samples
Known GenesCCDC178
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18040787
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