A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5593845



Internal ID21542436
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:1967786..1967975hg38UCSC Ensembl
chr19:1967785..1967974hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38190
hg19190
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17103421
SamplesHG00732
Known GenesCSNK1G2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5593845
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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