A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5615749



Internal ID21564054
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:141272528..141272528hg38UCSC Ensembl
chr3:140991370..140991370hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg38176
hg19176
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17133028
SamplesHG00512
Known GenesACPL2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5615749
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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