A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553592



Internal ID16341001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:18074268..18078015hg38UCSC Ensembl
Innerchr11:18095815..18099562hg19UCSC Ensembl
Innerchr11:18052391..18056138hg18UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg383748
hg193748
hg183748
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1667n54
Supporting Variantsnssv768333
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553592
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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