A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2909e59



Internal ID20129658
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:11252..68858hg38UCSC Ensembl
chr4:11252..68750hg19UCSC Ensembl
chr4:1252..58750hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3857607
hg1957499
hg1857499
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3351082, esv3349662, esv3331201, esv3326214, esv3337330, esv3365423
SamplesNA19239, NA12892, NA19238, NA12891, NA12878, NA19240
Known GenesZNF595, ZNF718
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv2909e59
Frequency
Sample Size185
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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