A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13965



Internal ID15834857
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:79975..79975hg38UCSC Ensembl
Outerchr6:78867..80045hg38UCSC Ensembl
Innerchr6:79975..79975hg19UCSC Ensembl
Outerchr6:78867..80045hg19UCSC Ensembl
Innerchr6:24975..24975hg18UCSC Ensembl
Outerchr6:23867..25045hg18UCSC Ensembl
Innerchr6:24975..24975hg17UCSC Ensembl
Outerchr6:23867..25045hg17UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg381179
hg191179
hg181179
hg171179
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv10796
Supporting Variants
SamplesNA18537
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)nssv13965
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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