A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553445



Internal ID16340854
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:8179758..8194306hg38UCSC Ensembl
Innerchr11:8201305..8215853hg19UCSC Ensembl
Innerchr11:8157881..8172429hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3814549
hg1914549
hg1814549
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1639n54
Supporting Variantsnssv767048
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553445
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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