A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1419529



Internal ID15236583
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:16131534..16134887hg38UCSC Ensembl
Innerchr7:16171159..16174512hg19UCSC Ensembl
Innerchr7:16137684..16141037hg18UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg383354
hg193354
hg183354
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv820033
Supporting Variants
SamplesAK1
Known GenesISPD
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)nssv1419529
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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