A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1419743



Internal ID15583527
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:57012364..57018287hg38UCSC Ensembl
Innerchr17:55089725..55095648hg19UCSC Ensembl
Innerchr17:52444724..52450647hg18UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg385924
hg195924
hg185924
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv819289
Supporting Variants
SamplesAK1
Known Genes
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)nssv1419743
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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