A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5655517



Internal ID21603822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:9477729..9477729hg38UCSC Ensembl
chr16:9571586..9571586hg19UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg38322
hg19322
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17082386
SamplesHG03371
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5655517
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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