A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5662426



Internal ID21610731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:34407386..34407386hg38UCSC Ensembl
chr17:32734405..32734405hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg38334
hg19334
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17093049
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5662426
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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