A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18173932



Internal ID20740972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:117708868..117709361hg38UCSC Ensembl
chr9:120471146..120471639hg19UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg38494
hg19494
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6454639
Supporting Variants
Samples
Known GenesTLR4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18173932
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00035


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