A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18035123



Internal ID20602163
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:35561800..35562104hg38UCSC Ensembl
chr17:33888819..33889123hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg38305
hg19305
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6512967
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18035123
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00875


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