A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5649468



Internal ID21597773
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:58013122..58013122hg38UCSC Ensembl
chr17:56090483..56090483hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg38114
hg19114
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17085590
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5649468
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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