A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv27306



Internal ID15497306
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:30236903..30247820hg38UCSC Ensembl
Outerchr15:30236101..30249402hg38UCSC Ensembl
Innerchr15:30529106..30540023hg19UCSC Ensembl
Outerchr15:30528304..30541605hg19UCSC Ensembl
Innerchr15:28316398..28327315hg18UCSC Ensembl
Outerchr15:28315596..28328897hg18UCSC Ensembl
Innerchr15:28316398..28327315hg17UCSC Ensembl
Outerchr15:28315596..28328897hg17UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg3813302
hg1913302
hg1813302
hg1713302
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9232
Supporting Variants
SamplesNA19221
Known Genes
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)nssv27306
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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