A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv10252



Internal ID15845215
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:14922792..14924582hg38UCSC Ensembl
Outerchr3:14964299..14966089hg19UCSC Ensembl
Outerchr3:14939303..14941093hg18UCSC Ensembl
Outerchr3:14939303..14941093hg17UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg381791
hg191791
hg181791
hg171791
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv12068
SamplesNA12155
Known GenesFGD5
MethodOligo aCGH
AnalysisStatistical threshold = 5.0, minimum +/- log2 ratio = 0.25 and minimum number of probes = 2
PlatformAgilent-015686 Custom Human 244K CGH Microarray
Comments
ReferencePerry_et_al_2008
Pubmed ID18304495
Accession Number(s)nsv10252
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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