A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17396776



Internal ID22454646
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:2084855..2090927hg38UCSC Ensembl
chr19:2084854..2090926hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg386073
hg196073
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5941038
Supporting Variants
Samples
Known GenesMOB3A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17396776
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001


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