A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv10355



Internal ID15845318
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:165565820..165605563hg38UCSC Ensembl
Outerchr3:165283608..165323351hg19UCSC Ensembl
Outerchr3:166766302..166806045hg18UCSC Ensembl
Outerchr3:166766310..166806053hg17UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg3839744
hg1939744
hg1839744
hg1739744
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv29243
SamplesNA19007
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)nsv10355
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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