A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18617



Internal ID15835749
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:63335523..63359931hg38UCSC Ensembl
Outerchr9:63335115..63367053hg38UCSC Ensembl
Innerchr9:67290495..67314903hg19UCSC Ensembl
Outerchr9:67290087..67322025hg19UCSC Ensembl
Innerchr9:66980315..67004723hg18UCSC Ensembl
Outerchr9:66979907..67011845hg18UCSC Ensembl
Innerchr9:65810737..65835145hg17UCSC Ensembl
Outerchr9:65810329..65842267hg17UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg3831939
hg1931939
hg1831939
hg1731939
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8497
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)nssv18617
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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