A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6516441



Internal ID20889802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:15692001..15722900hg38UCSC Ensembl
chr19:15802811..15833710hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3830900
hg1930900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3451n223
Supporting Variantsnssv18197648
Samples
Known GenesCYP4F12
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6516441
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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