A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv10363



Internal ID15845326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:177575216..177580181hg38UCSC Ensembl
Outerchr3:177293004..177297969hg19UCSC Ensembl
Outerchr3:178775698..178780663hg18UCSC Ensembl
Outerchr3:178775706..178780671hg17UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg384966
hg194966
hg184966
hg174966
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv11673, nssv29013
SamplesNA07048, NA10863
Known GenesLINC00578
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)nsv10363
Frequency
Sample Size31
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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