A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv611569



Internal ID16398978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:77565325..77618663hg38UCSC Ensembl
Innerchr8:78477561..78530899hg19UCSC Ensembl
Innerchr8:78640116..78693454hg18UCSC Ensembl
Cytoband8q21.12
Allele length
AssemblyAllele length
hg3853339
hg1953339
hg1853339
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12205n54
Supporting Variantsnssv1117010
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv611569
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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