A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv610466



Internal ID16051189
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:14469128..15809390hg38UCSC Ensembl
Innerchr8:14326637..15666899hg19UCSC Ensembl
Innerchr8:14371008..15711270hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg381340263
hg191340263
hg181340263
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1106813
Samples
Known GenesMIR383, SGCZ, TUSC3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv610466
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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