A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5659540



Internal ID21607845
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:17808414..17808414hg38UCSC Ensembl
chr17:17711728..17711728hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17080823
SamplesNA19239
Known GenesRAI1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5659540
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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