A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553443



Internal ID16340852
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:8178669..8190373hg38UCSC Ensembl
Innerchr11:8200216..8211920hg19UCSC Ensembl
Innerchr11:8156792..8168496hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3811705
hg1911705
hg1811705
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1639n54
Supporting Variantsnssv767046
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553443
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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