A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv24337



Internal ID15487086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34399518..34403767hg38UCSC Ensembl
Outerchr15:34398450..34405627hg38UCSC Ensembl
Innerchr15:34691719..34695968hg19UCSC Ensembl
Outerchr15:34690651..34697828hg19UCSC Ensembl
Innerchr15:32479011..32483260hg18UCSC Ensembl
Outerchr15:32477943..32485120hg18UCSC Ensembl
Innerchr15:32479011..32483260hg17UCSC Ensembl
Outerchr15:32477943..32485120hg17UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg387178
hg197178
hg187178
hg177178
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9241
Supporting Variants
SamplesNA18504
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)nssv24337
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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