A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv25295



Internal ID15833086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:22085403..22095457hg38UCSC Ensembl
Outerchr15:22084356..22095871hg38UCSC Ensembl
Innerchr15:22373354..22383408hg19UCSC Ensembl
Outerchr15:22372307..22383822hg19UCSC Ensembl
Innerchr15:19874718..19884772hg18UCSC Ensembl
Outerchr15:19873671..19885186hg18UCSC Ensembl
Innerchr15:19874718..19884772hg17UCSC Ensembl
Outerchr15:19873671..19885186hg17UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3811516
hg1911516
hg1811516
hg1711516
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9179
Supporting Variants
SamplesNA18502
Known GenesOR4N4
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)nssv25295
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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