A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17984154



Internal ID20551194
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:82362050..82382401hg38UCSC Ensembl
chr10:84121806..84142157hg19UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg3820352
hg1920352
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6442326
Supporting Variants
Samples
Known GenesNRG3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17984154
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0002


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