A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556467



Internal ID15997190
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:119154221..119193848hg38UCSC Ensembl
Innerchr11:119024931..119064558hg19UCSC Ensembl
Innerchr11:118530141..118569768hg18UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg3839628
hg1939628
hg1839628
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv784612
Samples
Known GenesABCG4, CCDC153, NLRX1, PDZD3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556467
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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