A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv22620



Internal ID15844184
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:41428845..41474611hg38UCSC Ensembl
Outerchr9:41428270..41475490hg38UCSC Ensembl
Innerchr9:45511868..45557634hg19UCSC Ensembl
Outerchr9:45511293..45558513hg19UCSC Ensembl
Innerchr9:45401864..45447630hg18UCSC Ensembl
Outerchr9:45401289..45448509hg18UCSC Ensembl
Innerchr9:44450804..44496570hg17UCSC Ensembl
Outerchr9:44450229..44497449hg17UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3847221
hg1947221
hg1847221
hg1747221
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8472
Supporting Variants
SamplesNA19221
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)nssv22620
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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