A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1419787



Internal ID15583571
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:38724491..38731150hg38UCSC Ensembl
InnerchrX:38583745..38590404hg19UCSC Ensembl
InnerchrX:38468689..38475348hg18UCSC Ensembl
CytobandXp11.4
Allele length
AssemblyAllele length
hg386660
hg196660
hg186660
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv819944
Supporting Variants
SamplesAK1
Known Genes
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)nssv1419787
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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