A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv8474



Internal ID15499700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:61838640..61875896hg38UCSC Ensembl
Outerchr9:46097769..46133823hg19UCSC Ensembl
Outerchr9:45987765..46023819hg18UCSC Ensembl
Outerchr9:44650514..44686568hg17UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3837257
hg1936055
hg1836055
hg1736055
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv21177, nssv16241, nssv18397, nssv19981, nssv17644, nssv22650
SamplesNA11830, NA10839, NA12872, NA19221, NA19132, NA19240
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)nsv8474
Frequency
Sample Size31
Observed Gain5
Observed Loss1
Observed Complex0
Frequencyn/a


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