A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv9267



Internal ID15500493
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:53528808..53840415hg38UCSC Ensembl
Outerchr15:53821005..54132612hg19UCSC Ensembl
Outerchr15:51608297..51919904hg18UCSC Ensembl
Outerchr15:51608297..51919904hg17UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38311608
hg19311608
hg18311608
hg17311608
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv26226
SamplesNA18860
Known GenesWDR72
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)nsv9267
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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