A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16274



Internal ID15834161
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:26885034..26892553hg38UCSC Ensembl
Outerchr6:26883977..26895668hg38UCSC Ensembl
Innerchr6:26852813..26860332hg19UCSC Ensembl
Outerchr6:26851756..26863447hg19UCSC Ensembl
Innerchr6:26960792..26968311hg18UCSC Ensembl
Outerchr6:26959735..26971426hg18UCSC Ensembl
Innerchr6:26960792..26968311hg17UCSC Ensembl
Outerchr6:26959735..26971426hg17UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg3811692
hg1911692
hg1811692
hg1711692
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv10806
Supporting Variants
SamplesNA18517
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)nssv16274
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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