A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17983183



Internal ID20550223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:59033601..59037900hg38UCSC Ensembl
chr10:60793361..60797660hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg384300
hg194300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6441261
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17983183
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