A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1418932



Internal ID15582716
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:118053903..118054291hg38UCSC Ensembl
Innerchr10:119813414..119813802hg19UCSC Ensembl
Innerchr10:119803404..119803792hg18UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg38389
hg19389
hg18389
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv819998
Supporting Variants
SamplesAK1
Known GenesCASC2
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)nssv1418932
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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