A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7087n54



Internal ID20140511
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:132915145..132916989hg38UCSC Ensembl
chr2:133672718..133674562hg19UCSC Ensembl
chr2:133389188..133391032hg18UCSC Ensembl
Cytoband2q21.2
Allele length
AssemblyAllele length
hg381845
hg191845
hg181845
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv583160, nsv583161, nsv583164, nsv583163, nsv583162
Samples
Known GenesMIR7853, NCKAP5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv7087n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss14
Observed Complex0
Frequencyn/a


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