A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv27267



Internal ID15496981
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:30198191..30213181hg38UCSC Ensembl
Outerchr15:30197342..30213514hg38UCSC Ensembl
Innerchr15:30490394..30505384hg19UCSC Ensembl
Outerchr15:30489545..30505717hg19UCSC Ensembl
Innerchr15:28277686..28292676hg18UCSC Ensembl
Outerchr15:28276837..28293009hg18UCSC Ensembl
Innerchr15:28277686..28292676hg17UCSC Ensembl
Outerchr15:28276837..28293009hg17UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg3816173
hg1916173
hg1816173
hg1716173
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9232
Supporting Variants
SamplesNA19221
Known GenesDKFZP434L187
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)nssv27267
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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