A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17809



Internal ID15837222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:122564063..122565486hg38UCSC Ensembl
Outerchr10:122563337..122566252hg38UCSC Ensembl
Innerchr10:124323579..124325002hg19UCSC Ensembl
Outerchr10:124322853..124325768hg19UCSC Ensembl
Innerchr10:124313569..124314992hg18UCSC Ensembl
Outerchr10:124312843..124315758hg18UCSC Ensembl
Innerchr10:124313569..124314992hg17UCSC Ensembl
Outerchr10:124312843..124315758hg17UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg382916
hg192916
hg182916
hg172916
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8730
Supporting Variants
SamplesNA18572
Known GenesDMBT1
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)nssv17809
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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