A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556611



Internal ID15997334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:134390175..134412392hg38UCSC Ensembl
Innerchr11:134260069..134282286hg19UCSC Ensembl
Innerchr11:133765279..133787496hg18UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3822218
hg1922218
hg1822218
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv785151
Samples
Known GenesB3GAT1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556611
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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