A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv832412



Internal ID9423263
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr12:52390206..52545452hg38UCSC Ensembl
Outerchr12:52783990..52939236hg19UCSC Ensembl
Outerchr12:51070257..51225503hg18UCSC Ensembl
Outerchr12:51070257..51225503hg17UCSC Ensembl
Cytoband12q13.13
Allele length
AssemblyAllele length
hg38155247
hg19155247
hg18155247
hg17155247
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1449834
Samples
Known GenesKRT5, KRT6A, KRT6B, KRT6C, KRT71, KRT75, KRT82
MethodBAC aCGH
AnalysisExperimental SDs (SDautosome) were calculated for each experiment on the basis of the log2 ratios of the 24,392 reliable clones minus the clones removed because of low signal-to-noise ratio (SNR) or high SD of replicate clone measures (SDclone). Thresholds for determining CNV clones were set at a multiple of the SDautosome value. For each experiment, clones were annotated as uninformative if they were filtered via SNR or SDclone, as a CNV loss if the log2 ratio was less than the negative threshold, as unchanged if the log2 ratio was between the negative and positive thresholds, and as a CNV gain if the log2 ratio was above the positive threshold.
PlatformGPL2616
Comments
ReferenceWong_et_al_2007
Pubmed ID17160897
Accession Number(s)nsv832412
Frequency
Sample Size95
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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