A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv22913



Internal ID15844305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:65218603..65229348hg38UCSC Ensembl
Outerchr9:65217290..65229424hg38UCSC Ensembl
Innerchr9:70362632..70373407hg19UCSC Ensembl
Outerchr9:70361319..70373483hg19UCSC Ensembl
Innerchr9:69602452..69613227hg18UCSC Ensembl
Outerchr9:69601139..69613303hg18UCSC Ensembl
Innerchr9:67871119..67881894hg17UCSC Ensembl
Outerchr9:67869806..67881970hg17UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg3812135
hg1912165
hg1812165
hg1712165
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8517
Supporting Variants
SamplesNA19221
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)nssv22913
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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