A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv8071



Internal ID15845983
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:24258846..24279810hg38UCSC Ensembl
Outerchr7:24298465..24319429hg19UCSC Ensembl
Outerchr7:24264990..24285954hg18UCSC Ensembl
Outerchr7:24071705..24092669hg17UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg3820965
hg1920965
hg1820965
hg1720965
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16932
SamplesNA18502
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)nsv8071
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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