A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1565n106



Internal ID22795393
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:22740295..22740365hg38UCSC Ensembl
chr18:20320258..20320328hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1111156, nsv1142913
SamplesKWS2, KWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv1565n106
Frequency
Sample Size2
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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