A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv819194



Internal ID15583895
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:22153462..23040894hg38UCSC Ensembl
Innerchr19:22336264..23223696hg19UCSC Ensembl
Innerchr19:22128104..23015536hg18UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38887433
hg19887433
hg18887433
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3n43
Supporting Variantsnssv1418808
SamplesAK1
Known GenesLOC100996349, LOC440518, ZNF492, ZNF676, ZNF728, ZNF729, ZNF98, ZNF99
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)nsv819194
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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