A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13884



Internal ID15840243
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:61325..62928hg38UCSC Ensembl
Innerchr6:61325..62928hg19UCSC Ensembl
Innerchr6:6325..7928hg18UCSC Ensembl
Innerchr6:6325..7928hg17UCSC Ensembl
Outerchr6:1..15669hg17UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg381604
hg191604
hg181604
hg1715669
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv10796
Supporting Variants
SamplesNA18975
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)nssv13884
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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