A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1402n100



Internal ID22787489
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:19847608..19943607hg38UCSC Ensembl
chr12:20000542..20096541hg19UCSC Ensembl
chr12:19891809..19987808hg18UCSC Ensembl
Cytoband12p12.2
Allele length
AssemblyAllele length
hg3896000
hg1996000
hg1896000
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1048862, nsv1040632
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)dgv1402n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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