A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18190739



Internal ID20757779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:82533973..82534422hg38UCSC Ensembl
chr9:85148888..85149337hg19UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg38450
hg19450
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6439374
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18190739
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00018


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