A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv554181



Internal ID16341590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:44092013..44094192hg38UCSC Ensembl
Innerchr11:44113563..44115742hg19UCSC Ensembl
Innerchr11:44070139..44072318hg18UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg382180
hg192180
hg182180
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv772169
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv554181
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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