A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv10527



Internal ID15845490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:76857109..76871833hg38UCSC Ensembl
Outerchr4:77778262..77792986hg19UCSC Ensembl
Outerchr4:77997286..78012010hg18UCSC Ensembl
Outerchr4:78135441..78150165hg17UCSC Ensembl
Cytoband4q21.1
Allele length
AssemblyAllele length
hg3814725
hg1914725
hg1814725
hg1714725
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13484
SamplesNA18517
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)nsv10527
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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