A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv25220



Internal ID15832565
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:21051231..21074696hg38UCSC Ensembl
Outerchr15:21049941..21075143hg38UCSC Ensembl
Innerchr15:21256560..21280025hg19UCSC Ensembl
Outerchr15:21255270..21280472hg19UCSC Ensembl
Innerchr15:19521219..19544684hg18UCSC Ensembl
Outerchr15:19519929..19545131hg18UCSC Ensembl
Innerchr15:19521219..19544684hg17UCSC Ensembl
Outerchr15:19519929..19545131hg17UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3825203
hg1925203
hg1825203
hg1725203
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9179
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)nssv25220
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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