A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv22717



Internal ID15831370
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:28298913..28318153hg38UCSC Ensembl
Outerchr15:28297938..28318698hg38UCSC Ensembl
Innerchr15:28544059..28563299hg19UCSC Ensembl
Outerchr15:28543084..28563844hg19UCSC Ensembl
Innerchr15:26217654..26236894hg18UCSC Ensembl
Outerchr15:26216679..26237439hg18UCSC Ensembl
Innerchr15:26217654..26236894hg17UCSC Ensembl
Outerchr15:26216679..26237439hg17UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg3820761
hg1920761
hg1820761
hg1720761
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9208
Supporting Variants
SamplesNA12740
Known GenesHERC2
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)nssv22717
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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