A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5663632



Internal ID21611937
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:113162428..113162428hg38UCSC Ensembl
chr13:113816742..113816742hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38630
hg19630
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17090514
SamplesNA24385
Known GenesPROZ
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5663632
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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