A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1395n100



Internal ID22787482
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:16010011..16051797hg38UCSC Ensembl
chr12:16162945..16204731hg19UCSC Ensembl
chr12:16054212..16095998hg18UCSC Ensembl
Cytoband12p12.3
Allele length
AssemblyAllele length
hg3841787
hg1941787
hg1841787
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1044455, nsv1050055
Samples
Known GenesDERA
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1395n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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