A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17390305



Internal ID22448175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:10634009..10661566hg38UCSC Ensembl
chr19:10744685..10772242hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3827558
hg1927558
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5936453
Supporting Variants
Samples
Known GenesILF3, ILF3-AS1, SLC44A2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17390305
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001


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