A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17985295



Internal ID20552335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:94731270..94864319hg38UCSC Ensembl
chr10:96491027..96624076hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg38133050
hg19133050
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6443122
Supporting Variants
Samples
Known GenesCYP2C18, CYP2C19
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17985295
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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