A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17381



Internal ID15485420
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:75784911..75941748hg38UCSC Ensembl
Outerchr10:75783922..75942865hg38UCSC Ensembl
Innerchr10:77544669..77701506hg19UCSC Ensembl
Outerchr10:77543680..77702623hg19UCSC Ensembl
Innerchr10:77214675..77371512hg18UCSC Ensembl
Outerchr10:77213686..77372629hg18UCSC Ensembl
Innerchr10:77214675..77371512hg17UCSC 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 StatusS
Merged Variantsnsv8689
Supporting Variants
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)nssv17381
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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