A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv554925



Internal ID15995648
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55607522..55634231hg38UCSC Ensembl
Innerchr11:55374998..55401707hg19UCSC Ensembl
Innerchr11:55131574..55158283hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3826710
hg1926710
hg1826710
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1910n54
Supporting Variantsnssv776581, nssv776579, nssv776580
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv554925
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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