A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1830n54



Internal ID22769725
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:54771612..54924512hg38UCSC Ensembl
chr11:51194768..51347668hg19UCSC Ensembl
chr11:51051344..51204244hg18UCSC Ensembl
Cytoband11p11.12
Allele length
AssemblyAllele length
hg38152901
hg19152901
hg18152901
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv554455, nsv554452
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1830n54
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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