A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17982250



Internal ID20549290
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:5965928..5967383hg38UCSC Ensembl
chr10:6007891..6009346hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg381456
hg191456
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6435708
Supporting Variants
Samples
Known GenesIL15RA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17982250
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00033


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer