A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv611836



Internal ID16399245
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:104752300..104866604hg38UCSC Ensembl
Innerchr8:105764528..105878832hg19UCSC Ensembl
Innerchr8:105833704..105948008hg18UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg38114305
hg19114305
hg18114305
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1156146
SamplesNINDS_171
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv611836
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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