A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1418573



Internal ID15583690
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:69738555..69747885hg38UCSC Ensembl
Innerchr6:70448447..70457777hg19UCSC Ensembl
Innerchr6:70505168..70514498hg18UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg389331
hg199331
hg189331
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv819863
Supporting Variants
SamplesAK1
Known GenesLMBRD1
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)nssv1418573
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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