A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6515917



Internal ID20889278
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:18211811..18225075hg38UCSC Ensembl
chr19:18322621..18335885hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg3813265
hg1913265
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18197721
Samples
Known GenesPDE4C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6515917
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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