A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6104589



Internal ID22013822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:14774674..14774674hg38UCSC Ensembl
chr19:14885486..14885486hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg38290
hg19290
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17622509
Samples
Known GenesEMR2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6104589
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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