A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv554913



Internal ID15995636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55606497..55639307hg38UCSC Ensembl
Innerchr11:55373973..55406783hg19UCSC Ensembl
Innerchr11:55130549..55163359hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3832811
hg1932811
hg1832811
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1912n54
Supporting Variantsnssv776525, nssv776524
Samples
Known GenesOR4P4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv554913
Frequency
Sample Size17421
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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