A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv20352



Internal ID15832832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:40167689..40195367hg38UCSC Ensembl
Outerchr9:40166554..40202967hg38UCSC Ensembl
Innerchr9:43161584..43189114hg19UCSC Ensembl
Outerchr9:43153944..43190249hg19UCSC Ensembl
Innerchr9:43151580..43179110hg18UCSC Ensembl
Outerchr9:43143940..43180245hg18UCSC Ensembl
Innerchr9:45462985..45490663hg17UCSC Ensembl
Outerchr9:45461850..45498263hg17UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3836414
hg1936306
hg1836306
hg1736414
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8483
Supporting Variants
SamplesNA18502
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)nssv20352
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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