A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1993n54



Internal ID20135417
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:70136867..70137406hg38UCSC Ensembl
chr11:69982973..69983512hg19UCSC Ensembl
chr11:69660621..69661160hg18UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg38540
hg19540
hg18540
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv555337, nsv555349, nsv555338, nsv555357
Samples
Known GenesANO1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1993n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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