A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18170014



Internal ID20737054
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:59103628..59104857hg38UCSC Ensembl
chr8:60016187..60017416hg19UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg381230
hg191230
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6431430
Supporting Variants
Samples
Known GenesTOX
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18170014
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