A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6522039



Internal ID20895400
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:3407201..3417800hg38UCSC Ensembl
chr19:3407199..3417798hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3810600
hg1910600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18197751
Samples
Known GenesNFIC
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6522039
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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