A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18408



Internal ID15836513
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:135322990..135325225hg38UCSC Ensembl
Outerchr9:135265841..135327327hg38UCSC Ensembl
Innerchr9:138214836..138217071hg19UCSC Ensembl
Outerchr9:138157687..138219173hg19UCSC Ensembl
Innerchr9:137354657..137356892hg18UCSC Ensembl
Outerchr9:137297508..137358994hg18UCSC Ensembl
Innerchr9:135440781..135443016hg17UCSC Ensembl
Outerchr9:135383632..135445118hg17UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3861487
hg1961487
hg1861487
hg1761487
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8578
Supporting Variants
SamplesNA18564
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)nssv18408
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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