A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17982811



Internal ID20549851
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:6294892..6299841hg38UCSC Ensembl
chr10:6336855..6341804hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg384950
hg194950
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6444662
Supporting Variants
Samples
Known GenesLOC399715
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17982811
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