A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv21804



Internal ID15839930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:101213310..101215844hg38UCSC Ensembl
Outerchr15:101212782..101219156hg38UCSC Ensembl
Innerchr15:101753515..101756049hg19UCSC Ensembl
Outerchr15:101752987..101759361hg19UCSC Ensembl
Innerchr15:99571038..99573572hg18UCSC Ensembl
Outerchr15:99570510..99576884hg18UCSC Ensembl
Innerchr15:99571038..99573572hg17UCSC Ensembl
Outerchr15:99570510..99576884hg17UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg386375
hg196375
hg186375
hg176375
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9309
Supporting Variants
SamplesNA18975
Known GenesCHSY1
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)nssv21804
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