A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv820163



Internal ID15584864
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:127391536..127393153hg38UCSC Ensembl
Innerchr7:127031590..127033207hg19UCSC Ensembl
Innerchr7:126818826..126820443hg18UCSC Ensembl
Cytoband7q31.33
Allele length
AssemblyAllele length
hg381618
hg191618
hg181618
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1419291
SamplesAK1
Known GenesZNF800
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)nsv820163
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer