A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv611579



Internal ID16398988
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:78934941..78952915hg38UCSC Ensembl
Innerchr8:79847176..79865150hg19UCSC Ensembl
Innerchr8:80009731..80027705hg18UCSC Ensembl
Cytoband8q21.12
Allele length
AssemblyAllele length
hg3817975
hg1917975
hg1817975
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1117021
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv611579
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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