A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5648349



Internal ID21596654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:2787264..2787264hg38UCSC Ensembl
chr16:2837265..2837265hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38364
hg19364
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17081194
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5648349
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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