A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv554398



Internal ID16341807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:50111161..50779592hg38UCSC Ensembl
Innerchr11:50070332..50738763hg19UCSC Ensembl
Innerchr11:50026908..50695339hg18UCSC Ensembl
Cytoband11p11.12
Allele length
AssemblyAllele length
hg38668432
hg19668432
hg18668432
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1815n54
Supporting Variantsnssv773972
Samples
Known GenesLOC441601, LOC646813
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv554398
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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