A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18043605



Internal ID20610645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:69290734..69291373hg38UCSC Ensembl
chr18:66957970..66958609hg19UCSC Ensembl
Cytoband18q22.2
Allele length
AssemblyAllele length
hg38640
hg19640
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6530330
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18043605
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0004


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