A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv20308



Internal ID15842387
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46710313..46710340hg38UCSC Ensembl
Outerchr10:46709971..46710808hg38UCSC Ensembl
Innerchr10:48109275..48109302hg19UCSC Ensembl
Outerchr10:48108933..48109770hg19UCSC Ensembl
Innerchr10:47729281..47729308hg18UCSC Ensembl
Outerchr10:47728939..47729776hg18UCSC Ensembl
Innerchr10:47729281..47729308hg17UCSC Ensembl
Outerchr10:47728939..47729776hg17UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38838
hg19838
hg18838
hg17838
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8636
Supporting Variants
SamplesNA19144
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)nssv20308
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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