A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14536



Internal ID15835340
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:26885034..26892330hg38UCSC Ensembl
Outerchr6:26883977..26892515hg38UCSC Ensembl
Innerchr6:26852813..26860109hg19UCSC Ensembl
Outerchr6:26851756..26860294hg19UCSC Ensembl
Innerchr6:26960792..26968088hg18UCSC Ensembl
Outerchr6:26959735..26968273hg18UCSC Ensembl
Innerchr6:26960792..26968088hg17UCSC Ensembl
Outerchr6:26959735..26968273hg17UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg388539
hg198539
hg188539
hg178539
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv10806
Supporting Variants
SamplesNA18552
Known GenesGUSBP2
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)nssv14536
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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