A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17785



Internal ID15840430
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:41428845..41482651hg38UCSC Ensembl
Outerchr9:41428270..41483822hg38UCSC Ensembl
Innerchr9:45511868..45565674hg19UCSC Ensembl
Outerchr9:45511293..45566844hg19UCSC Ensembl
Innerchr9:45401864..45455670hg18UCSC Ensembl
Outerchr9:45401289..45456840hg18UCSC Ensembl
Innerchr9:44450804..44504610hg17UCSC Ensembl
Outerchr9:44450229..44505780hg17UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3855553
hg1955552
hg1855552
hg1755552
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8472
Supporting Variants
SamplesNA18980
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)nssv17785
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