A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv819681



Internal ID15584382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:231462891..231463410hg38UCSC Ensembl
Innerchr2:232327602..232328121hg19UCSC Ensembl
Innerchr2:232035846..232036365hg18UCSC Ensembl
Cytoband2q37.1
Allele length
AssemblyAllele length
hg38520
hg19520
hg18520
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1418979
SamplesAK1
Known GenesNCL
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)nsv819681
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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