A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17985288



Internal ID20552328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:94678827..94872441hg38UCSC Ensembl
chr10:96438584..96632198hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg38193615
hg19193615
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6448831
Supporting Variants
Samples
Known GenesCYP2C18, CYP2C19
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17985288
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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