A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5662070



Internal ID21610375
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:58516148..58516148hg38UCSC Ensembl
chr16:58550052..58550052hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3885
hg1985
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17096336
SamplesNA12329
Known GenesSETD6
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5662070
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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