A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556640



Internal ID16344049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:134483933..134850279hg38UCSC Ensembl
Innerchr11:134353827..134720173hg19UCSC Ensembl
Innerchr11:133859037..134225383hg18UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38366347
hg19366347
hg18366347
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2207n54
Supporting Variantsnssv785183
Samples
Known GenesLOC283177
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556640
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