A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5653622



Internal ID21601927
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:48300336..48300336hg38UCSC Ensembl
chr13:48874472..48874472hg19UCSC Ensembl
Cytoband13q14.2
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17094234
SamplesHG01505
Known GenesLINC00441
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5653622
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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