A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18043355



Internal ID20610395
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:62288481..62289266hg38UCSC Ensembl
chr18:59955714..59956499hg19UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg38786
hg19786
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6532100
Supporting Variants
Samples
Known GenesKIAA1468
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18043355
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00036


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