A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv19808



Internal ID15830956
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46730130..46736238hg38UCSC Ensembl
Outerchr10:46729629..46736509hg38UCSC Ensembl
Innerchr10:46813379..46819487hg19UCSC Ensembl
Outerchr10:46813108..46819988hg19UCSC Ensembl
Innerchr10:46233385..46239493hg18UCSC Ensembl
Outerchr10:46233114..46239994hg18UCSC Ensembl
Innerchr10:46233385..46239493hg17UCSC Ensembl
Outerchr10:46233114..46239994hg17UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg386881
hg196881
hg186881
hg176881
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8636
Supporting Variants
SamplesNA12155
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)nssv19808
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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