A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv8022



Internal ID15845934
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:170623207..170736417hg38UCSC Ensembl
Outerchr6:170932295..171045505hg19UCSC Ensembl
Outerchr6:170774220..170887430hg18UCSC Ensembl
Outerchr6:170849927..170963137hg17UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38113211
hg19113211
hg18113211
hg17113211
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15015, nssv14675, nssv14947, nssv17121, nssv17113, nssv15546, nssv15304, nssv15569, nssv15539, nssv13849, nssv14230
SamplesNA11830, NA18504, NA12802, NA18860, NA10839, NA10847, NA10863, NA18572, NA18537, NA19173
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)nsv8022
Frequency
Sample Size31
Observed Gain3
Observed Loss7
Observed Complex0
Frequencyn/a


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