A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18192661



Internal ID20759701
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:86945301..86948900hg38UCSC Ensembl
chr9:89560216..89563815hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg383600
hg193600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6449701
Supporting Variants
Samples
Known GenesGAS1, LOC100506834
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18192661
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.02362


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