A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17616229



Internal ID21808276
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:25999786..25999786hg38UCSC Ensembl
chr15:26244933..26244933hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg38120
hg19120
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6084480
Supporting Variants
Samples
Known GenesLOC100128714
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17616229
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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