A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv10198



Internal ID15498475
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:151513554..151607130hg38UCSC Ensembl
Outerchr2:152370068..152463644hg19UCSC Ensembl
Outerchr2:152078314..152171890hg18UCSC Ensembl
Outerchr2:152195576..152289152hg17UCSC Ensembl
Cytoband2q23.3
Allele length
AssemblyAllele length
hg3893577
hg1993577
hg1893577
hg1793577
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv12210
SamplesNA19221
Known GenesNEB
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)nsv10198
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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