A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18190604



Internal ID20757644
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:24541876..24779926hg38UCSC Ensembl
chr9:24541874..24779924hg19UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg38238051
hg19238051
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6430547
Supporting Variants
Samples
Known GenesIZUMO3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18190604
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