A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv10305



Internal ID15845268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:107983280..107989555hg38UCSC Ensembl
Outerchr3:107702127..107708402hg19UCSC Ensembl
Outerchr3:109184817..109191092hg18UCSC Ensembl
Outerchr3:109184817..109191092hg17UCSC Ensembl
Cytoband3q13.12
Allele length
AssemblyAllele length
hg386276
hg196276
hg186276
hg176276
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv28915, nssv12164, nssv11849, nssv12042
SamplesNA18502, NA18517, NA19144, NA19173
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)nsv10305
Frequency
Sample Size31
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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