A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv826061



Internal ID6139101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:102449357..102449920hg19UCSC Ensembl
Innerchr11:101954567..101955130hg18UCSC Ensembl
Cytoband11q22.2
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1441359
SamplesNA18969
Known GenesMMP20
Method
AnalysisIdentical to variant call (no regions submitted)
PlatformAgilent 24M aCGH
Comments
ReferencePark_et_al_2010
Pubmed ID20364138
Accession Number(s)nsv826061
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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