A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv9473



Internal ID15500699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:87997925..88001562hg38UCSC Ensembl
Outerchr16:88031531..88035168hg19UCSC Ensembl
Outerchr16:86589032..86592669hg18UCSC Ensembl
Outerchr16:86589032..86592669hg17UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg383638
hg193638
hg183638
hg173638
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv22012, nssv24096
SamplesNA12740, NA18942
Known GenesBANP
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)nsv9473
Frequency
Sample Size31
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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