A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv21164



Internal ID15834387
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:62092869..62098869hg38UCSC Ensembl
Outerchr9:62084408..62098974hg38UCSC Ensembl
Innerchr9:67557287..67563287hg19UCSC Ensembl
Outerchr9:67557182..67571748hg19UCSC Ensembl
Innerchr9:67147107..67153107hg18UCSC Ensembl
Outerchr9:67147002..67161568hg18UCSC Ensembl
Innerchr9:66047445..66053440hg17UCSC Ensembl
Outerchr9:66047340..66061902hg17UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg3814567
hg1914567
hg1814567
hg1714563
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8499
Supporting Variants
SamplesNA18517
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)nssv21164
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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