A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv25905



Internal ID15486281
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34410815..34414846hg38UCSC Ensembl
Outerchr15:34409145..34416462hg38UCSC Ensembl
Innerchr15:34703016..34707047hg19UCSC Ensembl
Outerchr15:34701346..34708663hg19UCSC Ensembl
Innerchr15:32490308..32494339hg18UCSC Ensembl
Outerchr15:32488638..32495955hg18UCSC Ensembl
Innerchr15:32490308..32494339hg17UCSC Ensembl
Outerchr15:32488638..32495955hg17UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg387318
hg197318
hg187318
hg177318
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9241
Supporting Variants
SamplesNA18502
Known GenesGOLGA8A
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)nssv25905
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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