A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5971901



Internal ID22746836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:24229286..24229286hg38UCSC Ensembl
chr16:24240607..24240607hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg38179
hg19179
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17384292
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5971901
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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