A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1419699



Internal ID15236753
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:8356088..8361371hg38UCSC Ensembl
Innerchr1:8416148..8421431hg19UCSC Ensembl
Innerchr1:8338735..8344018hg18UCSC Ensembl
Cytoband1p36.23
Allele length
AssemblyAllele length
hg385284
hg195284
hg185284
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv819494
Supporting Variants
SamplesAK1
Known GenesRERE
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)nssv1419699
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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