A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1524n100



Internal ID22787611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:70043883..70181697hg38UCSC Ensembl
chr12:70437663..70575477hg19UCSC Ensembl
chr12:68723930..68861744hg18UCSC Ensembl
Cytoband12q15
Allele length
AssemblyAllele length
hg38137815
hg19137815
hg18137815
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1043649, nsv1035604
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1524n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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