A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv20528



Internal ID15483716
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:3653969..3654788hg38UCSC Ensembl
Outerchr11:3647916..3655190hg38UCSC Ensembl
Innerchr11:3675199..3676018hg19UCSC Ensembl
Outerchr11:3669146..3676420hg19UCSC Ensembl
Innerchr11:3631775..3632594hg18UCSC Ensembl
Outerchr11:3625722..3632996hg18UCSC Ensembl
Innerchr11:3631775..3632594hg17UCSC Ensembl
Outerchr11:3625722..3632996hg17UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg387275
hg197275
hg187275
hg177275
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8776
Supporting Variants
SamplesNA12155
Known GenesART1
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)nssv20528
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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