A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv8710



Internal ID15846622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:80857435..81100753hg38UCSC Ensembl
Outerchr10:82617191..82860509hg19UCSC Ensembl
Outerchr10:82607171..82850489hg18UCSC Ensembl
Outerchr10:82607171..82850489hg17UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg38243319
hg19243319
hg18243319
hg17243319
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv20167
SamplesNA11830
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)nsv8710
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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