A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv819621



Internal ID15237586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:89784895..89785200hg38UCSC Ensembl
Innerchr15:90328126..90328431hg19UCSC Ensembl
Innerchr15:88129130..88129435hg18UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38306
hg19306
hg18306
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1418582
SamplesAK1
Known GenesANPEP
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)nsv819621
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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