A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv10073



Internal ID15845036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:31982684..31986821hg38UCSC Ensembl
Outerchr1:32448285..32452422hg19UCSC Ensembl
Outerchr1:32220872..32225009hg18UCSC Ensembl
Outerchr1:32117378..32121515hg17UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg384138
hg194138
hg184138
hg174138
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16758
SamplesNA18564
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)nsv10073
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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