A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18172944



Internal ID20739984
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:83513101..83514300hg38UCSC Ensembl
chr8:84425336..84426535hg19UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg381200
hg191200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6426683
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18172944
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