A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18043974



Internal ID20611014
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:74930203..74930675hg38UCSC Ensembl
chr18:72642159..72642631hg19UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg38473
hg19473
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6525001
Supporting Variants
Samples
Known GenesZNF407
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18043974
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