A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18144019



Internal ID20711059
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:52747101..52828100hg38UCSC Ensembl
chr6:52611899..52692898hg19UCSC Ensembl
Cytoband6p12.2
Allele length
AssemblyAllele length
hg3881000
hg1981000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6415130
Supporting Variants
Samples
Known GenesGSTA1, GSTA2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18144019
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00013


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