A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv611087



Internal ID16398496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:40008372..40027055hg38UCSC Ensembl
Innerchr8:39865891..39884574hg19UCSC Ensembl
Innerchr8:39985048..40003731hg18UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg3818684
hg1918684
hg1818684
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1111257
Samples
Known GenesIDO2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv611087
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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