A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv819695



Internal ID15584396
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:47544710..47555030hg38UCSC Ensembl
Innerchr6:47512446..47522766hg19UCSC Ensembl
Innerchr6:47620405..47630725hg18UCSC Ensembl
Cytoband6p12.3
Allele length
AssemblyAllele length
hg3810321
hg1910321
hg1810321
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1418592
SamplesAK1
Known GenesCD2AP
MethodOligo aCGH
AnalysisThe array was scanned with Agilent DNA microarray scanner at 2 micron resolution. The resulting image was extracted by Agilent's Feature Extraction software. The log2 ratios were analyzed using NEXUS software. Each aberration call was manually checked to confirm the accuracy of the calls.
PlatformGSE19651
Comments
ReferenceKim_et_al_2009
Pubmed ID19587683
Accession Number(s)nsv819695
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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