A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154681



Internal ID22085186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:5250441..5252426hg38UCSC Ensembl
Outerchr11:5248100..5255848hg38UCSC Ensembl
Innerchr11:5271671..5273656hg19UCSC Ensembl
Outerchr11:5269330..5277078hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg387749
hg197749
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4005656
Samples
Known GenesHBG1, HBG2
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1154681
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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