A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv554020



Internal ID16341429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:37867896..37929110hg38UCSC Ensembl
Innerchr11:37889446..37950660hg19UCSC Ensembl
Innerchr11:37846022..37907236hg18UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3861215
hg1961215
hg1861215
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1174621
Samples1780862358_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv554020
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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