A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18236905



Internal ID20803945
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:99690031..99813799hg38UCSC Ensembl
chr7:99287654..99411422hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38123769
hg19123769
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6608309
Supporting Variants
Samples
Known GenesCYP3A4, CYP3A7, CYP3A7-CYP3AP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18236905
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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