A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15702



Internal ID15833163
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32646145..32655461hg38UCSC Ensembl
Outerchr6:32644864..32657037hg38UCSC Ensembl
Innerchr6:32613922..32623238hg19UCSC Ensembl
Outerchr6:32612641..32624814hg19UCSC Ensembl
Innerchr6:32721900..32731216hg18UCSC Ensembl
Outerchr6:32720619..32732792hg18UCSC Ensembl
Innerchr6:32721900..32731216hg17UCSC Ensembl
Outerchr6:32720619..32732792hg17UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3812174
hg1912174
hg1812174
hg1712174
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7883
Supporting Variants
SamplesNA18502
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)nssv15702
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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