A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5647770



Internal ID21596075
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:25040868..25040868hg38UCSC Ensembl
chr16:25052189..25052189hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg38358
hg19358
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17081256
SamplesHG02587
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5647770
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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