A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2656n223



Internal ID22805624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:101342587..101699627hg38UCSC Ensembl
chr15:101882792..102239830hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38357041
hg19357039
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6507902, nsv6499988
Samples
Known GenesPCSK6, TARSL2, TM2D3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv2656n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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