A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6443122



Internal ID21100675
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 StatusM
Merged Variants
Supporting Variantsnssv17985295
Samples
Known GenesCYP2C18, CYP2C19
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6443122
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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