A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5520240



Internal ID296574
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:2698192..2745173hg38UCSC Ensembl
chr19:2698190..2745171hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3846982
hg1946982
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17720442
Samples
Known GenesDIRAS1, GNG7, SLC39A3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5520240
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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