A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv555148



Internal ID15995871
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:59614833..59616350hg38UCSC Ensembl
Innerchr11:59382306..59383823hg19UCSC Ensembl
Innerchr11:59138882..59140399hg18UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg381518
hg191518
hg181518
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv777113, nssv777114
Samples
Known GenesOSBP
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv555148
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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