A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14826



Internal ID15482961
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:29949653..29950447hg38UCSC Ensembl
Outerchr6:29946931..29950971hg38UCSC Ensembl
Innerchr6:29917430..29918224hg19UCSC Ensembl
Outerchr6:29914708..29918748hg19UCSC Ensembl
Innerchr6:30025409..30026203hg18UCSC Ensembl
Outerchr6:30022687..30026727hg18UCSC Ensembl
Innerchr6:30025409..30026203hg17UCSC Ensembl
Outerchr6:30022687..30026727hg17UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg384041
hg194041
hg184041
hg174041
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv10810
Supporting Variants
SamplesNA10863
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)nssv14826
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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