A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1102n100



Internal ID22787189
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:38298550..38340379hg38UCSC Ensembl
chr11:38320100..38361929hg19UCSC Ensembl
chr11:38276676..38318505hg18UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3841830
hg1941830
hg1841830
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1039106, nsv1035444
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)dgv1102n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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