A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv554185



Internal ID16341594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:45367674..45393484hg38UCSC Ensembl
Innerchr11:45389225..45415035hg19UCSC Ensembl
Innerchr11:45345801..45371611hg18UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg3825811
hg1925811
hg1825811
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1175092
Samples1780862563_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv554185
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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