A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv819670



Internal ID15584371
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:167541553..167542253hg38UCSC Ensembl
Innerchr1:167510790..167511490hg19UCSC Ensembl
Innerchr1:165777414..165778114hg18UCSC Ensembl
Cytoband1q24.2
Allele length
AssemblyAllele length
hg38701
hg19701
hg18701
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1419063
SamplesAK1
Known GenesCREG1
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)nsv819670
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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