A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv21503



Internal ID15839519
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:62093602..62098974hg38UCSC Ensembl
Outerchr9:62093542..62099549hg38UCSC Ensembl
Innerchr9:67557182..67562554hg19UCSC Ensembl
Outerchr9:67556607..67562614hg19UCSC Ensembl
Innerchr9:67147002..67152374hg18UCSC Ensembl
Outerchr9:67146427..67152434hg18UCSC Ensembl
Innerchr9:66047340..66052707hg17UCSC Ensembl
Outerchr9:66046766..66052767hg17UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg386008
hg196008
hg186008
hg176002
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8499
Supporting Variants
SamplesNA18972
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)nssv21503
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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