A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2213n106



Internal ID22796041
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:11536617..11536982hg38UCSC Ensembl
chr20:11517265..11517630hg19UCSC Ensembl
Cytoband20p12.2
Allele length
AssemblyAllele length
hg38366
hg19366
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1135570, nsv1144258, nsv1130013
SamplesKWS2, KWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv2213n106
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