A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv823787



Internal ID6136827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:99270549..99302534hg19UCSC Ensembl
Innerchr6:99377270..99409255hg18UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Gain
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1428337
SamplesAK10
Known GenesPOU3F2
Method
AnalysisIdentical to variant call (no regions submitted)
PlatformAgilent 24M aCGH
Comments
ReferencePark_et_al_2010
Pubmed ID20364138
Accession Number(s)nsv823787
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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