A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv8549



Internal ID15846461
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:89560103..89564216hg38UCSC Ensembl
Outerchr9:92175018..92179131hg19UCSC Ensembl
Outerchr9:91364838..91368951hg18UCSC Ensembl
Outerchr9:89404572..89408685hg17UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg384114
hg194114
hg184114
hg174114
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv21051, nssv18025, nssv17032, nssv18196, nssv18525, nssv21563, nssv17544
SamplesNA18980, NA18860, NA18942, NA18975, NA18537, NA18972, NA18552
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)nsv8549
Frequency
Sample Size31
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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