A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556573



Internal ID16343982
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:130728318..130783840hg38UCSC Ensembl
Innerchr11:130598213..130653735hg19UCSC Ensembl
Innerchr11:130103423..130158945hg18UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg3855523
hg1955523
hg1855523
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv785109, nssv785108
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556573
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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