A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17816



Internal ID15841533
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:6613617..6622666hg38UCSC Ensembl
Outerchr10:6610263..6623506hg38UCSC Ensembl
Innerchr10:6655579..6664628hg19UCSC Ensembl
Outerchr10:6652225..6665468hg19UCSC Ensembl
Innerchr10:6695585..6704634hg18UCSC Ensembl
Outerchr10:6692231..6705474hg18UCSC Ensembl
Innerchr10:6695585..6704634hg17UCSC Ensembl
Outerchr10:6692231..6705474hg17UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3813244
hg1913244
hg1813244
hg1713244
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8601
Supporting Variants
SamplesNA19007
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)nssv17816
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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