A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18527



Internal ID15835727
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:61786232..61797134hg38UCSC Ensembl
Outerchr9:61785830..61798206hg38UCSC Ensembl
Innerchr9:45659076..45669982hg19UCSC Ensembl
Outerchr9:45658674..45671054hg19UCSC Ensembl
Innerchr9:45549072..45559978hg18UCSC Ensembl
Outerchr9:45548670..45561050hg18UCSC Ensembl
Innerchr9:65418395..65429301hg17UCSC Ensembl
Outerchr9:65417323..65429703hg17UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3812377
hg1912381
hg1812381
hg1712381
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8495
Supporting Variants
SamplesNA18563
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)nssv18527
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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