A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7302n54



Internal ID22775197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:222992836..223004741hg38UCSC Ensembl
chr2:223857554..223869459hg19UCSC Ensembl
chr2:223565798..223577703hg18UCSC Ensembl
Cytoband2q36.1
Allele length
AssemblyAllele length
hg3811906
hg1911906
hg1811906
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv584522, nsv584521
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv7302n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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