A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1418746



Internal ID15582530
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:143703652..143753212hg38UCSC Ensembl
Innerchr7:143400745..143450305hg19UCSC Ensembl
Innerchr7:143031678..143081238hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg3849561
hg1949561
hg1849561
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv819199
Supporting Variants
SamplesAK1
Known GenesFAM115C
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)nssv1418746
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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