A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv25320



Internal ID15833022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:22127499..22302101hg38UCSC Ensembl
Outerchr15:22127107..22302569hg38UCSC Ensembl
Innerchr15:22415450..22590052hg19UCSC Ensembl
Outerchr15:22415058..22590520hg19UCSC Ensembl
Innerchr15:19916814..20091416hg18UCSC Ensembl
Outerchr15:19916422..20091884hg18UCSC Ensembl
Innerchr15:19916814..20091416hg17UCSC Ensembl
Outerchr15:19916422..20091884hg17UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg38175463
hg19175463
hg18175463
hg17175463
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9179
Supporting Variants
SamplesNA18502
Known GenesREREP3
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)nssv25320
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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