A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv25556



Internal ID15495365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:32170005..32172982hg38UCSC Ensembl
Outerchr15:32169258..32173272hg38UCSC Ensembl
Innerchr15:32462206..32465183hg19UCSC Ensembl
Outerchr15:32461459..32465473hg19UCSC Ensembl
Innerchr15:30249498..30252475hg18UCSC Ensembl
Outerchr15:30248751..30252765hg18UCSC Ensembl
Innerchr15:30249498..30252475hg17UCSC Ensembl
Outerchr15:30248751..30252765hg17UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg384015
hg194015
hg184015
hg174015
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9238
Supporting Variants
SamplesNA19132
Known GenesCHRNA7
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)nssv25556
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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