A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv819785



Internal ID15584486
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:21978926..21984220hg38UCSC Ensembl
InnerchrX:21997044..22002338hg19UCSC Ensembl
InnerchrX:21906965..21912259hg18UCSC Ensembl
CytobandXp22.11
Allele length
AssemblyAllele length
hg385295
hg195295
hg185295
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1419700
SamplesAK1
Known GenesSMS
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)nsv819785
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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