A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1418759



Internal ID15582543
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:72461081..72461417hg38UCSC Ensembl
Innerchr5:71756908..71757244hg19UCSC Ensembl
Innerchr5:71792664..71793000hg18UCSC Ensembl
Cytoband5q13.2
Allele length
AssemblyAllele length
hg38337
hg19337
hg18337
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv819823
Supporting Variants
SamplesAK1
Known GenesZNF366
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)nssv1418759
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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