A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv24732



Internal ID15483966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:33937916..33973548hg38UCSC Ensembl
Outerchr16:33937450..33974567hg38UCSC Ensembl
Innerchr16:33740383..33776015hg19UCSC Ensembl
Outerchr16:33739917..33777034hg19UCSC Ensembl
Innerchr16:33647884..33683516hg18UCSC Ensembl
Outerchr16:33647418..33684535hg18UCSC Ensembl
Innerchr16:33647884..33683516hg17UCSC Ensembl
Outerchr16:33647418..33684535hg17UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg3837118
hg1937118
hg1837118
hg1737118
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9439
Supporting Variants
SamplesNA12155
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)nssv24732
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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