A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv19775



Internal ID15482391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34439409..34447178hg38UCSC Ensembl
Outerchr15:34438013..34449858hg38UCSC Ensembl
Innerchr15:34731610..34739379hg19UCSC Ensembl
Outerchr15:34730214..34742059hg19UCSC Ensembl
Innerchr15:32518902..32526671hg18UCSC Ensembl
Outerchr15:32517506..32529351hg18UCSC Ensembl
Innerchr15:32518902..32526671hg17UCSC Ensembl
Outerchr15:32517506..32529351hg17UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3811846
hg1911846
hg1811846
hg1711846
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9241
Supporting Variants
SamplesNA10847
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)nssv19775
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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