A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5646045



Internal ID21594350
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:71784606..71784606hg38UCSC Ensembl
chr17:69780747..69780747hg19UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17089566
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5646045
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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