A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv611234



Internal ID16398643
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:46149355..46768359hg38UCSC Ensembl
Innerchr8:47060977..47679981hg19UCSC Ensembl
Innerchr8:47180142..47799146hg18UCSC Ensembl
Cytoband8q11.1
Allele length
AssemblyAllele length
hg38619005
hg19619005
hg18619005
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1114125
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv611234
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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