A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv555189



Internal ID16342598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:64232109..64237321hg38UCSC Ensembl
Innerchr11:63999581..64004793hg19UCSC Ensembl
Innerchr11:63756157..63761369hg18UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg385213
hg195213
hg185213
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1964n54
Supporting Variantsnssv777151, nssv777152
Samples
Known GenesDNAJC4, VEGFB
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv555189
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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