A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1419032



Internal ID15236086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:58161127..58161754hg38UCSC Ensembl
Innerchr16:58195031..58195658hg19UCSC Ensembl
Innerchr16:56752532..56753159hg18UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg38628
hg19628
hg18628
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv819431
Supporting Variants
SamplesAK1
Known GenesCSNK2A2
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)nssv1419032
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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