A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv825373



Internal ID6138413
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:49616204..49617680hg19UCSC Ensembl
Innerchr10:49286210..49287686hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1421927
SamplesNA18997
Known GenesMAPK8
Method
AnalysisIdentical to variant call (no regions submitted)
PlatformAgilent 24M aCGH
Comments
ReferencePark_et_al_2010
Pubmed ID20364138
Accession Number(s)nsv825373
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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