A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv8445



Internal ID15499671
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:38283618..38685720hg38UCSC Ensembl
Outerchr9:38283615..38685717hg19UCSC Ensembl
Outerchr9:38273615..38675717hg18UCSC Ensembl
Outerchr9:38273615..38675717hg17UCSC Ensembl
Cytoband9p13.1
Allele length
AssemblyAllele length
hg38402103
hg19402103
hg18402103
hg17402103
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17566, nssv21900, nssv19722, nssv20543, nssv15791
SamplesNA18502, NA12872, NA19221, NA18972, NA18552
Known GenesALDH1B1, ANKRD18A, FAM201A, FAM95C, IGFBPL1
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)nsv8445
Frequency
Sample Size31
Observed Gain1
Observed Loss4
Observed Complex0
Frequencyn/a


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