A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5589015



Internal ID21537579
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:38687977..38688050hg38UCSC Ensembl
chr19:39178617..39178690hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17104674
SamplesHG00732
Known GenesACTN4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5589015
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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