A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7156n54



Internal ID18999332
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:167167818..167219111hg38UCSC Ensembl
chr2:168024328..168075621hg19UCSC Ensembl
chr2:167732574..167783867hg18UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg3851294
hg1951294
hg1851294
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv583590, nsv583589
Samples
Known GenesXIRP2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv7156n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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