A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv555992



Internal ID16343401
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:97178622..97372403hg38UCSC Ensembl
Innerchr11:97049622..97243403hg19UCSC Ensembl
Innerchr11:96554832..96748613hg18UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg38193782
hg19193782
hg18193782
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv781667
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv555992
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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