A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv8541



Internal ID15499767
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:83854808..83978843hg38UCSC Ensembl
Outerchr9:86469723..86593758hg19UCSC Ensembl
Outerchr9:85659543..85783578hg18UCSC Ensembl
Outerchr9:83699277..83823312hg17UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg38124036
hg19124036
hg18124036
hg17124036
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16391
SamplesNA12872
Known GenesC9orf64, HNRNPK, KIF27, MIR7-1
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)nsv8541
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