A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv819607



Internal ID15237572
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:43692441..43697048hg38UCSC Ensembl
Innerchr19:44196593..44201200hg19UCSC Ensembl
Innerchr19:48888433..48893040hg18UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg384608
hg194608
hg184608
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1419646
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)nsv819607
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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