A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv25575



Internal ID15838430
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20998839..21009226hg38UCSC Ensembl
Outerchr15:20998401..21011273hg38UCSC Ensembl
Innerchr15:21204168..21214555hg19UCSC Ensembl
Outerchr15:21203730..21216602hg19UCSC Ensembl
Innerchr15:19468827..19479214hg18UCSC Ensembl
Outerchr15:19468389..19481261hg18UCSC Ensembl
Innerchr15:19468827..19479214hg17UCSC Ensembl
Outerchr15:19468389..19481261hg17UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3812873
hg1912873
hg1812873
hg1712873
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9179
Supporting Variants
SamplesNA18860
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)nssv25575
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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