A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1419195



Internal ID15582979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:41139255..41140450hg38UCSC Ensembl
Innerchr6:41106993..41108188hg19UCSC Ensembl
Innerchr6:41214971..41216166hg18UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg381196
hg191196
hg181196
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv819921
Supporting Variants
SamplesAK1
Known GenesADCY10P1
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)nssv1419195
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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