A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv819969



Internal ID15237934
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:59706124..59706256hg38UCSC Ensembl
Innerchr10:61465882..61466014hg19UCSC Ensembl
Innerchr10:61135888..61136020hg18UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg38133
hg19133
hg18133
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1419103
SamplesAK1
Known GenesSLC16A9
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)nsv819969
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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