A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13150



Internal ID15831641
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:61325..70669hg38UCSC Ensembl
Outerchr6:60001..76709hg38UCSC Ensembl
Innerchr6:61325..70669hg19UCSC Ensembl
Outerchr6:60001..76709hg19UCSC Ensembl
Innerchr6:6325..15669hg18UCSC Ensembl
Outerchr6:5001..21709hg18UCSC Ensembl
Innerchr6:6325..15669hg17UCSC Ensembl
Outerchr6:1..21709hg17UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3816709
hg1916709
hg1816709
hg1721709
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv10796
Supporting Variants
SamplesNA12802
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)nssv13150
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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