A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv820918



Internal ID6111406
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:89398696..89400546hg19UCSC Ensembl
Innerchr15:87199700..87201550hg18UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Deletion
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1421138
SamplesNA10851
Known GenesACAN
Method
AnalysisIdentical to variant call (no regions submitted)
PlatformIllumina IIx
Comments
ReferenceJu_et_al_2010
Pubmed ID20802225
Accession Number(s)nsv820918
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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