A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553128



Internal ID16340537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:3244721..3338059hg38UCSC Ensembl
Innerchr11:3265951..3359289hg19UCSC Ensembl
Innerchr11:3222527..3315865hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3893339
hg1993339
hg1893339
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1577n54
Supporting Variantsnssv764561
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553128
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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