A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv822768



Internal ID6135808
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:147556986..147562654hg19UCSC Ensembl
Innerchr4:147776436..147782104hg18UCSC Ensembl
Cytoband4q31.22
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Gain
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1432794
SamplesNA18972
Known GenesPOU4F2
Method
AnalysisIdentical to variant call (no regions submitted)
PlatformAgilent 24M aCGH
Comments
ReferencePark_et_al_2010
Pubmed ID20364138
Accession Number(s)nsv822768
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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