A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16131



Internal ID15491943
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32042491..32042824hg38UCSC Ensembl
Outerchr6:32042149..32043263hg38UCSC Ensembl
Innerchr6:32010268..32010601hg19UCSC Ensembl
Outerchr6:32009926..32011040hg19UCSC Ensembl
Innerchr6:32118247..32118580hg18UCSC Ensembl
Outerchr6:32117905..32119019hg18UCSC Ensembl
Innerchr6:32118247..32118580hg17UCSC Ensembl
Outerchr6:32117905..32119019hg17UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg381115
hg191115
hg181115
hg171115
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv10824
Supporting Variants
SamplesNA18860
Known GenesTNXB
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)nssv16131
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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