A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv554173



Internal ID16341582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:43984709..43993819hg38UCSC Ensembl
Innerchr11:44006259..44015369hg19UCSC Ensembl
Innerchr11:43962835..43971945hg18UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg389111
hg199111
hg189111
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1773n54
Supporting Variantsnssv772152
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv554173
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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