A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18039909



Internal ID20606949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:31276589..31284869hg38UCSC Ensembl
chr18:28856552..28864832hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg388281
hg198281
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6519360
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18039909
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