A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17088216



Internal ID21504690
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:29257830..29257830hg38UCSC Ensembl
chr16:29269151..29269151hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38123
hg19123
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5652865
Supporting Variants
SamplesNA19240
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17088216
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer