A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18101135



Internal ID20668175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:25726056..25726601hg38UCSC Ensembl
chr3:25767547..25768092hg19UCSC Ensembl
Cytoband3p24.2
Allele length
AssemblyAllele length
hg38546
hg19546
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6360381
Supporting Variants
Samples
Known GenesNGLY1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18101135
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00018


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