A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5929558



Internal ID22704814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:10665693..10668733hg38UCSC Ensembl
chr19:10776369..10779409hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg383041
hg193041
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17398129
Samples
Known GenesILF3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5929558
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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