A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv819361



Internal ID15237326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:70146686..70147320hg38UCSC Ensembl
Innerchr6:70856578..70857212hg19UCSC Ensembl
Innerchr6:70913299..70913933hg18UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg38635
hg19635
hg18635
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1419034
SamplesAK1
Known GenesCOL19A1
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)nsv819361
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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