A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv819817



Internal ID15584518
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:100037355..100038287hg38UCSC Ensembl
Innerchr7:99634978..99635910hg19UCSC Ensembl
Innerchr7:99472914..99473846hg18UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38933
hg19933
hg18933
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1419125
SamplesAK1
Known GenesZKSCAN1
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)nsv819817
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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