A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv10600



Internal ID15845563
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:161272380..161284228hg38UCSC Ensembl
Outerchr4:162193532..162205380hg19UCSC Ensembl
Outerchr4:162412982..162424830hg18UCSC Ensembl
Outerchr4:162551137..162562985hg17UCSC Ensembl
Cytoband4q32.2
Allele length
AssemblyAllele length
hg3811849
hg1911849
hg1811849
hg1711849
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv12909
SamplesNA12740
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)nsv10600
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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