A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5652533



Internal ID21600838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:80538022..80538022hg38UCSC Ensembl
chr17:78511822..78511822hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3882
hg1982
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17082263
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5652533
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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