A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5650347



Internal ID21598652
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:65877600..65877600hg38UCSC Ensembl
chr16:65911503..65911503hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg384113
hg194113
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17088411
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5650347
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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