A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18044071



Internal ID20611112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:80225372..80241359hg38UCSC Ensembl
chr18:77983255..77999242hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg3815988
hg1915988
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6521326
Supporting Variants
Samples
Known GenesPARD6G
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18044071
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00082


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