A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18556



Internal ID15835323
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:45813929..45823586hg38UCSC Ensembl
Outerchr10:45813605..45825240hg38UCSC Ensembl
Innerchr10:46309377..46319034hg19UCSC Ensembl
Outerchr10:46309053..46320688hg19UCSC Ensembl
Innerchr10:45629383..45639040hg18UCSC Ensembl
Outerchr10:45629059..45640694hg18UCSC Ensembl
Innerchr10:45629383..45639040hg17UCSC Ensembl
Outerchr10:45629059..45640694hg17UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg3811636
hg1911636
hg1811636
hg1711636
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8630
Supporting Variants
SamplesNA18552
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)nssv18556
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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