A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18136874



Internal ID20703914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:106598901..106601400hg38UCSC Ensembl
chr6:107046776..107049275hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg382500
hg192500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6612939
Supporting Variants
Samples
Known GenesRTN4IP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18136874
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00031


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