A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv8776



Internal ID15500002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:3647916..3655190hg38UCSC Ensembl
Outerchr11:3669146..3676420hg19UCSC Ensembl
Outerchr11:3625722..3632996hg18UCSC Ensembl
Outerchr11:3625722..3632996hg17UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg387275
hg197275
hg187275
hg177275
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv20698, nssv19949, nssv19714, nssv20177, nssv22617, nssv18125, nssv17989, nssv19610, nssv19506, nssv19456, nssv20527, nssv21853, nssv20528, nssv19848, nssv19785, nssv19346, nssv22454, nssv24931, nssv17861, nssv22212, nssv18954, nssv23245, nssv20169, nssv17992, nssv18842
SamplesNA18502, NA11830, NA07029, NA18504, NA12155, NA18563, NA18860, NA18942, NA10839, NA18975, NA19007, NA10847, NA10863, NA12872, NA18572, NA19221, NA18537, NA18853, NA19132, NA18517, NA18564, NA19144, NA12740, NA19173, NA18552
Known GenesART1
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)nsv8776
Frequency
Sample Size31
Observed Gain3
Observed Loss22
Observed Complex0
Frequencyn/a


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