A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1964n54



Internal ID22769859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:64232057..64237321hg38UCSC Ensembl
chr11:63999529..64004793hg19UCSC Ensembl
chr11:63756105..63761369hg18UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg385265
hg195265
hg185265
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv555188, nsv555189, nsv555190
Samples
Known GenesDNAJC4, VEGFB
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1964n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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