A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18186343



Internal ID20753384
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:91921786..91933187hg38UCSC Ensembl
chr9:94684068..94695469hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg3811402
hg1911402
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6447993
Supporting Variants
Samples
Known GenesROR2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18186343
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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