A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv25567



Internal ID15832743
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:24441758..24476688hg38UCSC Ensembl
Outerchr15:24441205..24476997hg38UCSC Ensembl
Innerchr15:24686905..24721835hg19UCSC Ensembl
Outerchr15:24686352..24722144hg19UCSC Ensembl
Innerchr15:22237998..22272928hg18UCSC Ensembl
Outerchr15:22237445..22273237hg18UCSC Ensembl
Innerchr15:22237998..22272928hg17UCSC Ensembl
Outerchr15:22237445..22273237hg17UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3835793
hg1935793
hg1835793
hg1735793
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9195
Supporting Variants
SamplesNA18502
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)nssv25567
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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