A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv819656



Internal ID15237621
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:74247818..74254012hg38UCSC Ensembl
Innerchr7:73662148..73668342hg19UCSC Ensembl
Innerchr7:73300084..73306278hg18UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg386195
hg196195
hg186195
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1419757
SamplesAK1
Known GenesRFC2
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)nsv819656
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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