A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv819835



Internal ID15237800
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:148375914..148379330hg38UCSC Ensembl
Innerchr7:148073006..148076422hg19UCSC Ensembl
Innerchr7:147703939..147707355hg18UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg383417
hg193417
hg183417
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1419538
SamplesAK1
Known GenesCNTNAP2
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)nsv819835
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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