A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5659747



Internal ID21608052
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:8432347..8432347hg38UCSC Ensembl
chr17:8335665..8335665hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg38163
hg19163
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17100390, nssv17100389
SamplesHG03065, NA24385
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5659747
Frequency
Sample Size35
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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