A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1885n106



Internal ID20161242
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:33556218..33556554hg38UCSC Ensembl
chr2:33781285..33781621hg19UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg38337
hg19337
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1144908, nsv1112463
SamplesKWS1
Known GenesRASGRP3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv1885n106
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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