A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13971



Internal ID15838008
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:182630340..182632759hg38UCSC Ensembl
Outerchr4:182628609..182633466hg38UCSC Ensembl
Innerchr4:183551493..183553912hg19UCSC Ensembl
Outerchr4:183549762..183554619hg19UCSC Ensembl
Innerchr4:183788487..183790906hg18UCSC Ensembl
Outerchr4:183786756..183791613hg18UCSC Ensembl
Innerchr4:183926642..183929061hg17UCSC Ensembl
Outerchr4:183924911..183929768hg17UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg384858
hg194858
hg184858
hg174858
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv10620
Supporting Variants
SamplesNA18860
Known GenesTENM3
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)nssv13971
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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