A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556619



Internal ID16344028
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:134476225..134851577hg38UCSC Ensembl
Innerchr11:134346119..134721471hg19UCSC Ensembl
Innerchr11:133851329..134226681hg18UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38375353
hg19375353
hg18375353
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2207n54
Supporting Variantsnssv785158, nssv785159, nssv1176216
SamplesNINDS_135
Known GenesLOC283177
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556619
Frequency
Sample Size17421
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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