A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv21826



Internal ID15835580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:28656480..28657561hg38UCSC Ensembl
Outerchr15:28656380..28658130hg38UCSC Ensembl
Innerchr15:28901626..28902707hg19UCSC Ensembl
Outerchr15:28901526..28903276hg19UCSC Ensembl
Innerchr15:26700667..26701748hg18UCSC Ensembl
Outerchr15:26700567..26702317hg18UCSC Ensembl
Innerchr15:26700667..26701748hg17UCSC Ensembl
Outerchr15:26700567..26702317hg17UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg381751
hg191751
hg181751
hg171751
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9217
Supporting Variants
SamplesNA18552
Known GenesHERC2P9
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)nssv21826
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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