A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv8770



Internal ID15846682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:3235394..3338635hg38UCSC Ensembl
Outerchr11:3256624..3359865hg19UCSC Ensembl
Outerchr11:3213200..3316441hg18UCSC Ensembl
Outerchr11:3213200..3316441hg17UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38103242
hg19103242
hg18103242
hg17103242
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18035, nssv22557, nssv19476, nssv20497, nssv22364, nssv20668
SamplesNA11830, NA10847, NA10863, NA19132, NA18517, NA19144
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)nsv8770
Frequency
Sample Size31
Observed Gain2
Observed Loss4
Observed Complex0
Frequencyn/a


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