A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv20691



Internal ID15838609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:41502495..41505916hg38UCSC Ensembl
Outerchr9:41501534..41507090hg38UCSC Ensembl
Innerchr9:45585512..45588933hg19UCSC Ensembl
Outerchr9:45584551..45590107hg19UCSC Ensembl
Innerchr9:45475508..45478929hg18UCSC Ensembl
Outerchr9:45474547..45480103hg18UCSC Ensembl
Innerchr9:44524448..44527869hg17UCSC Ensembl
Outerchr9:44523487..44529043hg17UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg385557
hg195557
hg185557
hg175557
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8472
Supporting Variants
SamplesNA18860
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)nssv20691
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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