A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv19669



Internal ID15837189
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:22015979..22303333hg38UCSC Ensembl
Innerchr15:22303930..22591284hg19UCSC Ensembl
Innerchr15:19805294..20092648hg18UCSC Ensembl
Innerchr15:19805294..20092648hg17UCSC Ensembl
Outerchr15:19804866..20197782hg17UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg38287355
hg19287355
hg18287355
hg17392917
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9179
Supporting Variants
SamplesNA18572
Known GenesLOC727924, OR4M2, OR4N3P, OR4N4, REREP3
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)nssv19669
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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