A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5656390



Internal ID21604695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:2811282..2811282hg38UCSC Ensembl
chr16:2861283..2861283hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38125
hg19125
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17080554
SamplesHG02818
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5656390
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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