A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1400n100



Internal ID22787487
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:19575043..19683692hg38UCSC Ensembl
chr12:19727977..19836626hg19UCSC Ensembl
chr12:19619244..19727893hg18UCSC Ensembl
Cytoband12p12.3
Allele length
AssemblyAllele length
hg38108650
hg19108650
hg18108650
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1050454, nsv1040158
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)dgv1400n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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