A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5647610



Internal ID21595915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:1967793..1967793hg38UCSC Ensembl
chr19:1967792..1967792hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38305
hg19305
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17103422
SamplesHG03065
Known GenesCSNK1G2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5647610
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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