A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv21651



Internal ID15491376
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:45906217..45913380hg38UCSC Ensembl
Outerchr10:45905818..45913641hg38UCSC Ensembl
Innerchr10:46401665..46408828hg19UCSC Ensembl
Outerchr10:46401266..46409089hg19UCSC Ensembl
Innerchr10:45721671..45728834hg18UCSC Ensembl
Outerchr10:45721272..45729095hg18UCSC Ensembl
Innerchr10:45721671..45728834hg17UCSC Ensembl
Outerchr10:45721272..45729095hg17UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg387824
hg197824
hg187824
hg177824
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8631
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)nssv21651
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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