A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6516669



Internal ID20890030
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 StatusM
Merged Variantsdgv3524n223
Supporting Variantsnssv18048026
Samples
Known GenesCYP2B6, CYP2B7P, CYP2G1P
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6516669
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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