A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv21144



Internal ID15840196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20996806..20999794hg38UCSC Ensembl
Outerchr15:20996708..21001063hg38UCSC Ensembl
Innerchr15:21202135..21205123hg19UCSC Ensembl
Outerchr15:21202037..21206392hg19UCSC Ensembl
Innerchr15:19466794..19469782hg18UCSC Ensembl
Outerchr15:19466696..19471051hg18UCSC Ensembl
Innerchr15:19466794..19469782hg17UCSC Ensembl
Outerchr15:19466696..19471051hg17UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg384356
hg194356
hg184356
hg174356
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9179
Supporting Variants
SamplesNA18975
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)nssv21144
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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