A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2634n223



Internal ID22805602
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:96329501..96335500hg38UCSC Ensembl
chr15:96872730..96878729hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg386000
hg196000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6510544, nsv6513896
Samples
Known GenesMIR1469, NR2F2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv2634n223
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