A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv8766



Internal ID15499992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:2971449..3205956hg38UCSC Ensembl
Outerchr11:2992679..3227186hg19UCSC Ensembl
Outerchr11:2949255..3183762hg18UCSC Ensembl
Outerchr11:2949255..3183762hg17UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38234508
hg19234508
hg18234508
hg17234508
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18005, nssv18782, nssv19580, nssv19713, nssv21823, nssv22334, nssv21901, nssv24851, nssv22527, nssv19919
SamplesNA07029, NA18504, NA07048, NA10847, NA19221, NA18853, NA19132, NA18517, NA19240, NA19173
Known GenesCARS, NAP1L4, OSBPL5
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)nsv8766
Frequency
Sample Size31
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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