A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv20029



Internal ID15837297
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:51329665..51330228hg38UCSC Ensembl
Outerchr15:51327401..51331034hg38UCSC Ensembl
Innerchr15:51621862..51622425hg19UCSC Ensembl
Outerchr15:51619598..51623231hg19UCSC Ensembl
Innerchr15:49409154..49409717hg18UCSC Ensembl
Outerchr15:49406890..49410523hg18UCSC Ensembl
Innerchr15:49409154..49409717hg17UCSC Ensembl
Outerchr15:49406890..49410523hg17UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg383634
hg193634
hg183634
hg173634
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9265
Supporting Variants
SamplesNA18572
Known GenesCYP19A1
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)nssv20029
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer