A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv19270



Internal ID15831884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:22085872..22093424hg38UCSC Ensembl
Outerchr15:22085403..22094379hg38UCSC Ensembl
Innerchr15:22373823..22381375hg19UCSC Ensembl
Outerchr15:22373354..22382330hg19UCSC Ensembl
Innerchr15:19875187..19882739hg18UCSC Ensembl
Outerchr15:19874718..19883694hg18UCSC Ensembl
Innerchr15:19875187..19882739hg17UCSC Ensembl
Outerchr15:19874718..19883694hg17UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg388977
hg198977
hg188977
hg178977
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9179
Supporting Variants
SamplesNA12802
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)nssv19270
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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