A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18180779



Internal ID20747819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:80171494..80189775hg38UCSC Ensembl
chr9:82786409..82804690hg19UCSC Ensembl
Cytoband9q21.31
Allele length
AssemblyAllele length
hg3818282
hg1918282
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6444867
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18180779
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