A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv611216



Internal ID16398625
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:43975689..43983626hg38UCSC Ensembl
Innerchr8:43830832..43838769hg19UCSC Ensembl
Innerchr8:43949989..43957926hg18UCSC Ensembl
Cytoband8p11.1
Allele length
AssemblyAllele length
hg387938
hg197938
hg187938
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1114091
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv611216
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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