A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv555969



Internal ID16343378
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:96120930..96187835hg38UCSC Ensembl
Innerchr11:95854094..95920999hg19UCSC Ensembl
Innerchr11:95493742..95560647hg18UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg3866906
hg1966906
hg1866906
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv781562
Samples
Known GenesMAML2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv555969
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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