A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv611847



Internal ID16399256
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:106826664..106860349hg38UCSC Ensembl
Innerchr8:107838892..107872577hg19UCSC Ensembl
Innerchr8:107908068..107941753hg18UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg3833686
hg1933686
hg1833686
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1156147
SamplesHGDP00515
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv611847
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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