A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5656199



Internal ID21604504
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:4663600..4663600hg38UCSC Ensembl
chr19:4663612..4663612hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17105346
SamplesHG00732
Known GenesC19orf10
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5656199
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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