A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18175904



Internal ID20742944
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:20802223..20849183hg38UCSC Ensembl
chr9:20802222..20849182hg19UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3846961
hg1946961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6426527
Supporting Variants
Samples
Known GenesFOCAD
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18175904
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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