A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18175086



Internal ID20742126
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:114938001..114941000hg38UCSC Ensembl
chr9:117700281..117703280hg19UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg383000
hg193000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6437723
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18175086
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