A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv555275



Internal ID15995998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:67734155..67839059hg38UCSC Ensembl
Innerchr11:67501626..67606530hg19UCSC Ensembl
Innerchr11:67258202..67363106hg18UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg38104905
hg19104905
hg18104905
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv778611
Samples
Known GenesFAM86C2P
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv555275
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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