A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv8689



Internal ID15499915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:75783922..75942865hg38UCSC Ensembl
Outerchr10:77543680..77702623hg19UCSC Ensembl
Outerchr10:77213686..77372629hg18UCSC Ensembl
Outerchr10:77213686..77372629hg17UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg38158944
hg19158944
hg18158944
hg17158944
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17381
SamplesNA12872
Known GenesC10orf11
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)nsv8689
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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