A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv10532



Internal ID15845495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:88287027..88289014hg38UCSC Ensembl
Outerchr4:89208179..89210166hg19UCSC Ensembl
Outerchr4:89427203..89429190hg18UCSC Ensembl
Outerchr4:89565358..89567345hg17UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg381988
hg191988
hg181988
hg171988
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13467
SamplesNA19132
Known Genes
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)nsv10532
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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