A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2381n106



Internal ID20161738
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:33402694..33403794hg38UCSC Ensembl
chr21:34775000..34776100hg19UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg381101
hg191101
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1126607, nsv1122041
SamplesKWS2, KWS1
Known GenesIFNGR2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv2381n106
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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