A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv20032



Internal ID15838974
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20048005..20070509hg38UCSC Ensembl
Outerchr15:20047638..20071940hg38UCSC Ensembl
Innerchr15:20253258..20275762hg19UCSC Ensembl
Outerchr15:20252891..20277193hg19UCSC Ensembl
Innerchr15:18513272..18535776hg18UCSC Ensembl
Outerchr15:18512905..18537207hg18UCSC Ensembl
Innerchr15:18513272..18535776hg17UCSC Ensembl
Outerchr15:18512905..18537207hg17UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg3824303
hg1924303
hg1824303
hg1724303
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9179
Supporting Variants
SamplesNA18942
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)nssv20032
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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