A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1089n100



Internal ID22787176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:31556967..31650138hg38UCSC Ensembl
chr11:31578514..31671686hg19UCSC Ensembl
chr11:31535090..31628262hg18UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg3893172
hg1993173
hg1893173
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1048175, nsv1053469
Samples
Known GenesELP4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1089n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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