A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv827768



Internal ID6132858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:79615278..79640094hg19UCSC Ensembl
Innerchr16:78172779..78197595hg18UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Gain
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1428693
SamplesAK10
Known GenesMAF
Method
AnalysisIdentical to variant call (no regions submitted)
PlatformAgilent 24M aCGH
Comments
ReferencePark_et_al_2010
Pubmed ID20364138
Accession Number(s)nsv827768
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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