A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv22833



Internal ID15830797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20626192..20626550hg38UCSC Ensembl
Outerchr15:20625069..20627173hg38UCSC Ensembl
Innerchr15:20831495..20831853hg19UCSC Ensembl
Outerchr15:20830372..20832476hg19UCSC Ensembl
Innerchr15:19091509..19091867hg18UCSC Ensembl
Outerchr15:19090386..19092490hg18UCSC Ensembl
Innerchr15:19091509..19091867hg17UCSC Ensembl
Outerchr15:19090386..19092490hg17UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg382105
hg192105
hg182105
hg172105
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9179
Supporting Variants
SamplesNA12155
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)nssv22833
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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