A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15129



Internal ID15831478
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:26883977..26901114hg38UCSC Ensembl
Outerchr6:26883163..26902053hg38UCSC Ensembl
Innerchr6:26851756..26868893hg19UCSC Ensembl
Outerchr6:26850942..26869832hg19UCSC Ensembl
Innerchr6:26959735..26976872hg18UCSC Ensembl
Outerchr6:26958921..26977811hg18UCSC Ensembl
Innerchr6:26959735..26976872hg17UCSC Ensembl
Outerchr6:26958921..26977811hg17UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg3818891
hg1918891
hg1818891
hg1718891
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv10806
Supporting Variants
SamplesNA12740
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)nssv15129
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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