A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3290n106



Internal ID20162647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:24811628..24817743hg38UCSC Ensembl
chr6:24811856..24817971hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg386116
hg196116
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1112120, nsv1120883
SamplesKWS1, KWS2
Known GenesFAM65B
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv3290n106
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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