A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv27369



Internal ID15497528
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:32196863..32245159hg38UCSC Ensembl
Outerchr15:32196730..32245432hg38UCSC Ensembl
Innerchr15:32489064..32537360hg19UCSC Ensembl
Outerchr15:32488931..32537633hg19UCSC Ensembl
Innerchr15:30276356..30324652hg18UCSC Ensembl
Outerchr15:30276223..30324925hg18UCSC Ensembl
Innerchr15:30276356..30324652hg17UCSC Ensembl
Outerchr15:30276223..30324925hg17UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg3848703
hg1948703
hg1848703
hg1748703
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9238
Supporting Variants
SamplesNA19221
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)nssv27369
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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