A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17391593



Internal ID22449463
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:46134382..46240983hg38UCSC Ensembl
chr19:46637639..46744240hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg38106602
hg19106602
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5928409
Supporting Variants
Samples
Known GenesDKFZp434J0226, IGFL1, IGFL2, RNU6-66P
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17391593
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001


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