A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv24385



Internal ID15829825
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:55774017..55777486hg38UCSC Ensembl
Outerchr16:55773308..55778455hg38UCSC Ensembl
Innerchr16:55807929..55811398hg19UCSC Ensembl
Outerchr16:55807220..55812367hg19UCSC Ensembl
Innerchr16:54365430..54368899hg18UCSC Ensembl
Outerchr16:54364721..54369868hg18UCSC Ensembl
Innerchr16:54365430..54368899hg17UCSC Ensembl
Outerchr16:54364721..54369868hg17UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg385148
hg195148
hg185148
hg175148
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9445
Supporting Variants
SamplesNA11830
Known GenesCES1P1
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)nssv24385
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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