A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18174020



Internal ID20741060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:118257801..118259800hg38UCSC Ensembl
chr9:121020079..121022078hg19UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg382000
hg192000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6438020
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18174020
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00049


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