A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6521022



Internal ID20894383
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:49540406..49586977hg38UCSC Ensembl
chr19:50043663..50090234hg19UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg3846572
hg1946572
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18198252
Samples
Known GenesNOSIP, PRRG2, RCN3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6521022
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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