A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16792



Internal ID15838767
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:67151037..67162013hg38UCSC Ensembl
Outerchr9:67145160..67162322hg38UCSC Ensembl
Innerchr9:40530828..40541804hg19UCSC Ensembl
Outerchr9:40530519..40547681hg19UCSC Ensembl
Innerchr9:40520828..40531804hg18UCSC Ensembl
Outerchr9:40520519..40537681hg18UCSC Ensembl
Innerchr9:40260111..40271087hg17UCSC Ensembl
Outerchr9:40259802..40276964hg17UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg3817163
hg1917163
hg1817163
hg1717163
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8456
Supporting Variants
SamplesNA18942
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)nssv16792
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