A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17544



Internal ID15840024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:89561334..89562695hg38UCSC Ensembl
Outerchr9:89560103..89564216hg38UCSC Ensembl
Innerchr9:92176249..92177610hg19UCSC Ensembl
Outerchr9:92175018..92179131hg19UCSC Ensembl
Innerchr9:91366069..91367430hg18UCSC Ensembl
Outerchr9:91364838..91368951hg18UCSC Ensembl
Innerchr9:89405803..89407164hg17UCSC Ensembl
Outerchr9:89404572..89408685hg17UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg384114
hg194114
hg184114
hg174114
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8549
Supporting Variants
SamplesNA18975
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)nssv17544
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