A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv554396



Internal ID16341805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:50098683..50683379hg38UCSC Ensembl
Innerchr11:50057854..50642550hg19UCSC Ensembl
Innerchr11:50014430..50599126hg18UCSC Ensembl
Cytoband11p11.12
Allele length
AssemblyAllele length
hg38584697
hg19584697
hg18584697
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1814n54
Supporting Variantsnssv1174301
SamplesHGDP00519
Known GenesLOC441601, LOC646813
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv554396
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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