A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5657888



Internal ID21606193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:21177331..21177331hg38UCSC Ensembl
chr16:21188652..21188652hg19UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg38314
hg19314
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17084710
SamplesHG02011
Known GenesTMEM159
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5657888
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