A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv10224



Internal ID15498501
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:234051054..234053740hg38UCSC Ensembl
Outerchr2:234959698..234962384hg19UCSC Ensembl
Outerchr2:234624437..234627123hg18UCSC Ensembl
Outerchr2:234741698..234744384hg17UCSC Ensembl
Cytoband2q37.1
Allele length
AssemblyAllele length
hg382687
hg192687
hg182687
hg172687
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv29145, nssv28634
SamplesNA18980, NA18564
Known GenesSPP2
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)nsv10224
Frequency
Sample Size31
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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