A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1249n100



Internal ID20152865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:87802086..88022773hg38UCSC Ensembl
chr11:87512978..87755941hg19UCSC Ensembl
chr11:87190626..87395589hg18UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg38220688
hg19242964
hg18204964
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1048411, nsv1036593
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)dgv1249n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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