A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv19961



Internal ID15832114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:22160305..22180700hg38UCSC Ensembl
Outerchr15:22157595..22181400hg38UCSC Ensembl
Innerchr15:22448256..22468651hg19UCSC Ensembl
Outerchr15:22445546..22469351hg19UCSC Ensembl
Innerchr15:19949620..19970015hg18UCSC Ensembl
Outerchr15:19946910..19970715hg18UCSC Ensembl
Innerchr15:19949620..19970015hg17UCSC Ensembl
Outerchr15:19946910..19970715hg17UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3823806
hg1923806
hg1823806
hg1723806
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9179
Supporting Variants
SamplesNA12872
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)nssv19961
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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