A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv24873



Internal ID15841744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20021518..20022937hg38UCSC Ensembl
Outerchr15:20021018..20023331hg38UCSC Ensembl
Innerchr15:20226771..20228190hg19UCSC Ensembl
Outerchr15:20226271..20228584hg19UCSC Ensembl
Innerchr15:18486785..18488204hg18UCSC Ensembl
Outerchr15:18486285..18488598hg18UCSC Ensembl
Innerchr15:18486785..18488204hg17UCSC Ensembl
Outerchr15:18486285..18488598hg17UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg382314
hg192314
hg182314
hg172314
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9179
Supporting Variants
SamplesNA19132
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)nssv24873
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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