A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv554486



Internal ID16341895
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:54715977..54771612hg38UCSC Ensembl
Innerchr11:51347668..51403303hg19UCSC Ensembl
Innerchr11:51204244..51259879hg18UCSC Ensembl
Cytoband11p11.12
Allele length
AssemblyAllele length
hg3855636
hg1955636
hg1855636
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1842n54
Supporting Variantsnssv774220
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv554486
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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