A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5663561



Internal ID21611866
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:56993088..56993088hg38UCSC Ensembl
chr16:57027000..57027000hg19UCSC Ensembl
Cytoband16q13
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17084833
SamplesHG03683
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5663561
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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