A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv20922



Internal ID15486003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:42551846..42556300hg38UCSC Ensembl
Outerchr10:42551366..42556848hg38UCSC Ensembl
Innerchr10:43047294..43051748hg19UCSC Ensembl
Outerchr10:43046814..43052296hg19UCSC Ensembl
Innerchr10:42367300..42371754hg18UCSC Ensembl
Outerchr10:42366820..42372302hg18UCSC Ensembl
Innerchr10:42367300..42371754hg17UCSC Ensembl
Outerchr10:42366820..42372302hg17UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg385483
hg195483
hg185483
hg175483
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8625
Supporting Variants
SamplesNA18502
Known GenesZNF37BP
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)nssv20922
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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