A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv24978



Internal ID15841686
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:21028166..21035213hg38UCSC Ensembl
Outerchr15:21027666..21049941hg38UCSC Ensembl
Innerchr15:21233495..21240542hg19UCSC Ensembl
Outerchr15:21232995..21255270hg19UCSC Ensembl
Innerchr15:19498154..19505201hg18UCSC Ensembl
Outerchr15:19497654..19519929hg18UCSC Ensembl
Innerchr15:19498154..19505201hg17UCSC Ensembl
Outerchr15:19497654..19519929hg17UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3822276
hg1922276
hg1822276
hg1722276
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)nssv24978
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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