A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv21620



Internal ID15837730
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:23174518..23189557hg38UCSC Ensembl
Outerchr15:23174492..23190651hg38UCSC Ensembl
Innerchr15:22683511..22698550hg19UCSC Ensembl
Outerchr15:22682417..22698899hg19UCSC Ensembl
Innerchr15:20234875..20249914hg18UCSC Ensembl
Outerchr15:20233781..20250263hg18UCSC Ensembl
Innerchr15:20234875..20249914hg17UCSC Ensembl
Outerchr15:20233781..20250263hg17UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3816160
hg1916483
hg1816483
hg1716483
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9181
Supporting Variants
SamplesNA18853
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)nssv21620
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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