A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1418996



Internal ID15582780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:149254332..149254872hg38UCSC Ensembl
Innerchr7:148951423..148951963hg19UCSC Ensembl
Innerchr7:148582356..148582896hg18UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg38541
hg19541
hg18541
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv819456
Supporting Variants
SamplesAK1
Known GenesZNF212
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)nssv1418996
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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