A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1214n100



Internal ID19011582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:67552445..67996597hg38UCSC Ensembl
chr11:67319916..67764068hg19UCSC Ensembl
chr11:67076492..67520644hg18UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg38444153
hg19444153
hg18444153
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1043487, nsv1041988, nsv1050463, nsv1053811, nsv1047236, nsv1038189
Samples
Known GenesACY3, ALDH3B2, DOC2GP, FAM86C2P, GSTP1, NDUFV1, NUDT8, TBX10, UNC93B1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1214n100
Frequency
Sample Size29084
Observed Gain7
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer