A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3111n223



Internal ID22806079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:41093195..41118292hg38UCSC Ensembl
chr17:39249447..39274544hg19UCSC Ensembl
Cytoband17q21.2
Allele length
AssemblyAllele length
hg3825098
hg1925098
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6495787, nsv6499605
Samples
Known GenesKRTAP4-11, KRTAP4-8, KRTAP4-9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv3111n223
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