A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5658904



Internal ID21607209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:68697437..68697437hg38UCSC Ensembl
chr17:66693578..66693578hg19UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg38335
hg19335
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17084495
SamplesNA18534
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5658904
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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