A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6608309



Internal ID20981380
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 StatusM
Merged Variants
Supporting Variantsnssv18236905
Samples
Known GenesCYP3A4, CYP3A7, CYP3A7-CYP3AP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6608309
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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