A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv22070



Internal ID15491033
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:30522532..30522676hg38UCSC Ensembl
Outerchr15:30522195..30523061hg38UCSC Ensembl
Innerchr15:30814735..30814879hg19UCSC Ensembl
Outerchr15:30814398..30815264hg19UCSC Ensembl
Innerchr15:28602027..28602171hg18UCSC Ensembl
Outerchr15:28601690..28602556hg18UCSC Ensembl
Innerchr15:28602027..28602171hg17UCSC Ensembl
Outerchr15:28601690..28602556hg17UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg38867
hg19867
hg18867
hg17867
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9232
Supporting Variants
SamplesNA18853
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)nssv22070
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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