A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv23787



Internal ID15843229
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:28205553..28207410hg38UCSC Ensembl
Outerchr16:28203740..28208499hg38UCSC Ensembl
Innerchr16:28216874..28218731hg19UCSC Ensembl
Outerchr16:28215061..28219820hg19UCSC Ensembl
Innerchr16:28124375..28126232hg18UCSC Ensembl
Outerchr16:28122562..28127321hg18UCSC Ensembl
Innerchr16:28124375..28126232hg17UCSC Ensembl
Outerchr16:28122562..28127321hg17UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg384760
hg194760
hg184760
hg174760
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9410
Supporting Variants
SamplesNA19173
Known GenesXPO6
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)nssv23787
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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