A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv9292



Internal ID15847204
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:85182753..85237857hg38UCSC Ensembl
Outerchr15:85725984..85781088hg19UCSC Ensembl
Outerchr15:83526988..83582092hg18UCSC Ensembl
Outerchr15:83526988..83582092hg17UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg3855105
hg1955105
hg1855105
hg1755105
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv22276, nssv26365
SamplesNA18860, NA18552
Known GenesLOC440300, LOC642423
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)nsv9292
Frequency
Sample Size31
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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