A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6527434



Internal ID20900795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:15647304..15664381hg38UCSC Ensembl
chr19:15758114..15775191hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3817078
hg1917078
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18197640
Samples
Known GenesCYP4F3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6527434
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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