A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv819505



Internal ID8551195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:60645976..60646588hg38UCSC Ensembl
Innerchr14:61112694..61113306hg19UCSC Ensembl
Innerchr14:60182447..60183059hg18UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg38613
hg19613
hg18613
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1419027
SamplesAK1
Known GenesSIX1
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)nsv819505
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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