A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5646475



Internal ID21594780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:16197975..16197975hg38UCSC Ensembl
chr19:16308786..16308786hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17103227
SamplesNA19238
Known GenesAP1M1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5646475
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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