A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv23120



Internal ID15829797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:28659223..28663413hg38UCSC Ensembl
Outerchr15:28658610..28664300hg38UCSC Ensembl
Innerchr15:28904369..28908559hg19UCSC Ensembl
Outerchr15:28903756..28909446hg19UCSC Ensembl
Innerchr15:26703410..26707600hg18UCSC Ensembl
Outerchr15:26702797..26708487hg18UCSC Ensembl
Innerchr15:26703410..26707600hg17UCSC Ensembl
Outerchr15:26702797..26708487hg17UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg385691
hg195691
hg185691
hg175691
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9217
Supporting Variants
SamplesNA11830
Known GenesHERC2P9
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)nssv23120
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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