A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18185651



Internal ID20752691
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:92355786..92425176hg38UCSC Ensembl
chr9:95118068..95187458hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg3869391
hg1969391
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6447714
Supporting Variants
Samples
Known GenesCENPP, OGN, OMD
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18185651
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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