A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18615



Internal ID15835071
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:5692350..5693354hg38UCSC Ensembl
Outerchr10:5691728..5694764hg38UCSC Ensembl
Innerchr10:5734313..5735317hg19UCSC Ensembl
Outerchr10:5733691..5736727hg19UCSC Ensembl
Innerchr10:5774319..5775323hg18UCSC Ensembl
Outerchr10:5773697..5776733hg18UCSC Ensembl
Innerchr10:5774319..5775323hg17UCSC Ensembl
Outerchr10:5773697..5776733hg17UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg383037
hg193037
hg183037
hg173037
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8600
Supporting Variants
SamplesNA18537
Known GenesFAM208B
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)nssv18615
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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