A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv8652



Internal ID15499878
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:45948800..45951843hg38UCSC Ensembl
Outerchr10:51643980..51647026hg19UCSC Ensembl
Outerchr10:51313986..51317032hg18UCSC Ensembl
Outerchr10:51313986..51317032hg17UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg383044
hg193047
hg183047
hg173047
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv22671
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)nsv8652
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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