A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14158



Internal ID15842736
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:61325..76741hg38UCSC Ensembl
Outerchr6:60001..77093hg38UCSC Ensembl
Innerchr6:61325..76741hg19UCSC Ensembl
Outerchr6:60001..77093hg19UCSC Ensembl
Innerchr6:6325..21741hg18UCSC Ensembl
Outerchr6:5001..22093hg18UCSC Ensembl
Innerchr6:6325..21741hg17UCSC Ensembl
Outerchr6:1..22093hg17UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3817093
hg1917093
hg1817093
hg1722093
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv10796
Supporting Variants
SamplesNA19144
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)nssv14158
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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