A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3024n54



Internal ID18995200
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:132303883..132305655hg38UCSC Ensembl
chr12:132880469..132882241hg19UCSC Ensembl
chr12:131390542..131392314hg18UCSC Ensembl
Cytoband12q24.33
Allele length
AssemblyAllele length
hg381773
hg191773
hg181773
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv560983, nsv560992, nsv560995, nsv560989, nsv560985, nsv560984
Samples
Known GenesGALNT9
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3024n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss17
Observed Complex0
Frequencyn/a


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