A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv611484



Internal ID16398893
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:69854816..69942974hg38UCSC Ensembl
Innerchr8:70767051..70855209hg19UCSC Ensembl
Innerchr8:70929605..71017763hg18UCSC Ensembl
Cytoband8q13.3
Allele length
AssemblyAllele length
hg3888159
hg1988159
hg1888159
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1115775
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv611484
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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