A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv10084



Internal ID15845047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:34608858..34615458hg38UCSC Ensembl
Outerchr1:35074459..35081059hg19UCSC Ensembl
Outerchr1:34847046..34853646hg18UCSC Ensembl
Outerchr1:34743552..34750152hg17UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg386601
hg196601
hg186601
hg176601
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13436
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)nsv10084
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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