A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv21471



Internal ID15838005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:6613617..6621811hg38UCSC Ensembl
Outerchr10:6610263..6622040hg38UCSC Ensembl
Innerchr10:6655579..6663773hg19UCSC Ensembl
Outerchr10:6652225..6664002hg19UCSC Ensembl
Innerchr10:6695585..6703779hg18UCSC Ensembl
Outerchr10:6692231..6704008hg18UCSC Ensembl
Innerchr10:6695585..6703779hg17UCSC Ensembl
Outerchr10:6692231..6704008hg17UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3811778
hg1911778
hg1811778
hg1711778
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8601
Supporting Variants
SamplesNA18860
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)nssv21471
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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