A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5651235



Internal ID21599540
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:32238009..32238009hg38UCSC Ensembl
chr17:30565028..30565028hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg38173
hg19173
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17096851
SamplesHG03065
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5651235
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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