A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv819342



Internal ID15584043
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:31550570..31552433hg38UCSC Ensembl
Innerchr7:31590184..31592047hg19UCSC Ensembl
Innerchr7:31556709..31558572hg18UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg381864
hg191864
hg181864
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1419345
SamplesAK1
Known GenesCCDC129
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)nsv819342
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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