A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1392n100



Internal ID22787479
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:12366385..12389934hg38UCSC Ensembl
chr12:12519319..12542868hg19UCSC Ensembl
chr12:12410586..12434135hg18UCSC Ensembl
Cytoband12p13.2
Allele length
AssemblyAllele length
hg3823550
hg1923550
hg1823550
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1047762, nsv1050133, nsv1042425, nsv1049869
Samples
Known GenesLOH12CR1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1392n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss14
Observed Complex0
Frequencyn/a


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