A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18723



Internal ID15827986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:64562647..64563995hg38UCSC Ensembl
Outerchr9:64561873..64564574hg38UCSC Ensembl
Innerchr9:69575065..69576413hg19UCSC Ensembl
Outerchr9:69574291..69576992hg19UCSC Ensembl
Innerchr9:68864885..68866233hg18UCSC Ensembl
Outerchr9:68864111..68866812hg18UCSC Ensembl
Innerchr9:67477941..67479289hg17UCSC Ensembl
Outerchr9:67477167..67479868hg17UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg382702
hg192702
hg182702
hg172702
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8514
Supporting Variants
SamplesNA07048
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)nssv18723
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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