A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7814n54



Internal ID22775709
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:33247140..33254349hg38UCSC Ensembl
chr21:34619445..34626654hg19UCSC Ensembl
chr21:33541315..33548524hg18UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg387210
hg197210
hg187210
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv587374, nsv587375
Samples
Known GenesIFNAR2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv7814n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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