A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5739n223



Internal ID22808707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:43507101..43529639hg38UCSC Ensembl
chr5:43507203..43529741hg19UCSC Ensembl
Cytoband5p12
Allele length
AssemblyAllele length
hg3822539
hg1922539
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6377972, nsv6391858
Samples
Known GenesC5orf34, PAIP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv5739n223
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