A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18048026



Internal ID20615066
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:40883097..41028609hg38UCSC Ensembl
chr19:41389002..41534514hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38145513
hg19145513
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6516669
Supporting Variants
Samples
Known GenesCYP2B6, CYP2B7P, CYP2G1P
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18048026
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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